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WO2003047506A2 - Peptides agonistes d'antigenes specifiques de la prostate et leurs utilisations - Google Patents

Peptides agonistes d'antigenes specifiques de la prostate et leurs utilisations Download PDF

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Publication number
WO2003047506A2
WO2003047506A2 PCT/US2002/037805 US0237805W WO03047506A2 WO 2003047506 A2 WO2003047506 A2 WO 2003047506A2 US 0237805 W US0237805 W US 0237805W WO 03047506 A2 WO03047506 A2 WO 03047506A2
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WIPO (PCT)
Prior art keywords
psa
seq
peptide
amino acid
cells
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PCT/US2002/037805
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English (en)
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WO2003047506A3 (fr
Inventor
Jeffrey Schlom
Kwong-Yok Tsang
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The Government Of The United States Of America, Represented By The Secretary, Department Of Health And Human Services
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Priority to DE60235041T priority Critical patent/DE60235041D1/de
Priority to AT02789873T priority patent/ATE454447T1/de
Priority to CA2468258A priority patent/CA2468258C/fr
Priority to AU2002352913A priority patent/AU2002352913B2/en
Priority to JP2003548767A priority patent/JP4364643B2/ja
Priority to EP02789873A priority patent/EP1461073B1/fr
Priority to DK02789873.3T priority patent/DK1461073T3/da
Priority to US10/497,003 priority patent/US7247615B2/en
Publication of WO2003047506A2 publication Critical patent/WO2003047506A2/fr
Publication of WO2003047506A3 publication Critical patent/WO2003047506A3/fr

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    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14—Hydrolases (3)
    • C12N9/48—Hydrolases (3) acting on peptide bonds (3.4)
    • C12N9/50—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25)
    • C12N9/64—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from animal tissue
    • C12N9/6421—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from animal tissue from mammals
    • C12N9/6424—Serine endopeptidases (3.4.21)
    • C12N9/6445—Kallikreins (3.4.21.34; 3.4.21.35)
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/08—Drugs for disorders of the urinary system of the prostate
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Definitions

  • the present invention relates to isolated peptides comprising agonist epitopes of prostate-specific antigen (PSA), h one aspect, this invention relates to peptides comprising agonist epitopes of the PSA-3 CTL (cytotoxic T lymphocyte) epitope.
  • PSA-3 CTL cytotoxic T lymphocyte
  • the invention also relates to nucleic acids (e.g., recombinant viral vectors) encoding peptides that comprise PSA-3 agonist epitopes, as well as host cells comprising these nucleic acids, and antibodies that bind to these peptides.
  • compositions comprising the nucleic acids and peptides of the invention, as well as methods of treatment of prostate cancer employing such compositions, e.g., peptide-mediated and vector- mediated iminunotherapy.
  • PSA Prostate-specific antigen
  • HLA-A2 binding peptide was used to monitor patients who were positive for the HLA-A2 allele. Patients possessing the HLA-A2 allele were chosen for monitoring because it is the most common HLA allele in individuals in North America and is expressed by approximately 50% of the Caucasian population (J. Lee, 1990, "The HLA system: a new approach” Proceedings Of The First Red Cross International Histocompatibility Workshop Springer Verlag, New York, p. 154).
  • the PSA-3 peptide was subsequently used in the ELISPOT assay to monitor immune responses in vaccinated patients (J.P. Eder et al., 2000, Clin. Cancer Res. 6:1632- 1638; P. Arlen et al., 2000, Cancer Immuno. Immunother. 49:517-529).
  • the results of these studies indicated that increases in precursor frequencies observed in the ELISPOT assay as a result of vaccination with rV-PSA were relatively modest (i.e., 2- to 4-fold) (J.P. Eder et al., 2000, Clin. Cancer Res. 6:1632-1638).
  • the present invention therefore describes compositions and methods for increasing
  • the immunogenicity of PSA peptides was increased by modifying the amino acid residues that interact with HLA molecules.
  • Previous studies have shown that amino acid modification in the anchor residues ⁇ /peptides may result in enhanced binding to MHC and enhanced T cell activation, while other amino acid modifications will have no effect or act to antagonize T cell activation (H.M. Grey et al., 1995, Cancer Surv. 22:37-49; M.T. De Magistris et al., 1992, Cell 68:625-632; S.C. Jameson et al., 1995, Immunity 2:1-11; S. Zaremba et al., 1997, Cancer Res. 57:4570- 4577).
  • Enhancement of T cell activation by modifying HLA-anchor residues has been demonstrated for some human melanoma-associated antigens (D. Valmori et al., 1998, J. Immunol. 160:1750-1758, 1998; Y. Kawakami, Y., Eliyahu et al., 1995, J. Immunol. 154:3961-3968), but has not been demonstrated for antigens associated with most solid tumors, leukemias, or lymphonias.
  • T cells stimulated with dendritic cells (DCs) pulsed with PSA-3A peptide produced higher levels of IFN-7 than DCs pulsed with PSA-3 peptide.
  • DCs dendritic cells
  • no increase in apoptosis was observed in T cells stimulated with the PSA-3 A agonist as 15 compared with those stimulated with PSA- 3.
  • human T cell lines generated with the PSA-3 A agonist had the ability to lyse human prostate carcinoma cells expressing native PSA in an MHC-A2 restricted manner.
  • recombinant vaccinia viruses were constructed containing the entire PSA transgene with or without the single amino acid change that constitutes the PSA-3A epitope.
  • DCs infected with the recombinant vector contaimng the agonist amino acid change within the entire PSA gene were more effective than the rV-PSA vector in enhancing IFN- ⁇ production by T Attorney Docket No. : 38163-0166
  • the PSA-3A agonist was shown to induce higher levels of T cell activation, as compared with the PSA-3 peptide, in an in vivo model using HLA-A2.1/Kb transgenic mice (strain reported by A. Vitiello et al, 1991, J. Exp. Med. 173:1007-1015; V. H. Engelhard et al, 1991, J. Immunol.6:l226-l232). Accordingly, the PSA-3A agonist epitope of this invention is useful for both peptide-mediated and vector-mediated immunotherapy protocols for prostate cancer.
  • the invention provides isolated PSA-3 agonist peptides (e.g., SEQ ID NO:3-SEQ ID NO:5), as well as polypeptides (e.g., PSA polypeptides) comprising one or more of these peptides, and fragments and variants thereof. Also provided are methods of making these peptides and polypeptides.
  • the invention also provides isolated nucleic acids (e.g., SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20-SEQ ID NO:20
  • PSA-3 agonist peptides e.g., PSA polypeptides
  • polypeptides e.g., PSA polypeptides
  • fragments or variants thereof This invention also provides probes, primers, and vectors comprising these nucleotide sequences, as well as host cells comprising these vectors.
  • nucleic acids are also provided. Also provided are methods of making these nucleic acids, as well as methods for making the probes, primers, vectors, and host cells of the invention.
  • the invention also provides antibodies and antibody fragments that bind to PSA-3 agonist peptides (e.g., SEQ TD NO:3SEQ ID NO:5), or polypeptides (e.g., PSA polypeptides) comprising these peptides, or variants, or fragments thereof.
  • PSA-3 agonist peptides e.g., SEQ TD NO:3SEQ ID NO:5
  • polypeptides e.g., PSA polypeptides
  • the invention also provides methods of making these antibodies and antibody fragments.
  • the invention also provides methods of identifying test agents that can be used as drugs to further enhance immunoreactivity to PSA-3 agonist peptides. Such agents may act as mimetics of PSA-3 agonist peptides, or may enhance the formation or stability of peptide-HLA complexes.
  • the invention also provides diagnostic reagents comprising antibodies or antibody fragments that bind to PSA-3 agonist peptides, polypeptides, or fragments or variants thereof. Further provided are diagnostic reagents comprising PSA-3 agonist Attorney Docket No. : 38163-0166
  • polynucleotides are also provided. Also provided are methods of using these reagents to monitor the vector- based, cell-based, and or peptide-based immunotherapies of the invention.
  • the invention also provides pharmaceutical compositions comprising one or more PSA-3 agonist peptides, PSA-3 agonist-modified vectors, or PSA-3 agonist-modified host cells.
  • the invention further provides methods of admimsfration of these pharmaceutical compositions for the treatment of prostate cancer.
  • Such treatments include vector- mediated, cell-mediated, and peptide-mediated immunotherapies, and combinations thereof.
  • the treatments of the invention can be used alone, or in conjunction with traditional cancer therapies, e.g., surgery, radiation therapy, and/or chemotherapy. Additional objects and advantages afforded by this invention will be apparent from the detailed description and exemplification herein below.
  • FIGS 1A-1B Binding of PSA peptides to HLA-A2. Peptides were analyzed for binding to the T2A2 cell line as described in the Examples section. Peptides were used at concentrations of 0 to 50 ⁇ g/ml (Figure 1A) and lower concentrations (Figure IB).
  • PSA-3 is the parental PSA peptide (open triangles).
  • PSA-3 L-155; also called PSA-3A) (solid squares), PSA-3 (Y154) (solid circles), PSA-3 (Y154/L155) (solid triangles) and PSA-3 (LI 63) (open squares) are PSA-3 agonist peptides.
  • NCA peptide (open circles) is a negative control. Results are expressed in relative fluorescence values (MFI).
  • FIG. 1 Comparison of the stability of the complex of the PSA-3 or PSA-3A peptide with HLA-A2.
  • T2A2 cells were incubated with PSA-3 (open squares) or PSA-3A (closed squares) peptide at a concentration of 50 ⁇ ,g/ml overnight and then washed free of unbound peptide and incubated with brefeldin A to block delivery of new class I molecules to cell surface. At indicated times, cells were stained for the presence of surface peptide-HLA-A2 complexes. Results are expressed in relative % binding as compared to 100% binding at time zero. Attorney Docket No.: 38163-0166
  • FIGS 3A-3B Cytotoxicity of the T-PSA-3A T cell line derived by pulsing PBMCs with the PSA-3A peptide ( Figure 3A), and the T-PSA-3 T cell line derived by pulsing PBMCs with the PSA-3 peptide ( Figure 3B).
  • Target cells were Cl R-A2 cells pulsed with either PSA-3 A (solid squares) or PSA-3 (solid circles) peptide at a concentration of 25 ⁇ g/ml for in vitro stimulation (IVS-3) at various E:T (Effector: target) ratios.
  • Cl R-A2 cells with no peptide (open squares) were also tested.
  • Cytotoxic T lymphocyte (CTL) activity was determined in an 18-h m In release assay.
  • Figures 5A-5C DNA fragmentation in peptide stimulated T cells using the TUNEL assay. Apoptosis of CD8 + cells activated by PSA peptide pulsed autologous B cells.
  • Figure 5A T-PSA-3 cells stimulated with B cells with no peptide
  • Figure 5B T- PSA-3 cells stimulated with B cells pulsed with PSA-3 peptide
  • Figure 5C T-PSA-3 cells stimulated with B cells pulsed with PSA-3A peptide. Numbers in each histogram indicate percent of apoptotic cells (cells above line) as described in the Examples section.
  • FIGS. 6A-6F Cytometric Bead Array assay for the production of cytokines by peptide-stimulated T cells.
  • the production of IL-2, IL-4, IL-5, IL-10, TNF- ⁇ , and TFN- ⁇ (from top to bottom from each figure) was analyzed.
  • Standards at concentrations of each cytokine at 0 pg/ml ( Figure 6A), 312 pg/ml ( Figure 6B), and 5000 pg/ml ( Figure 6C) were used to determine the concentrations of these six cytokines in the samples.
  • Supernatant obtained from T-PSA-3 cells + APC (autologous B cells) with no peptide Figure 6D
  • Supernatant obtained from T-PSA-3 + APC + PSA3A Figure 6E
  • Supernatant obtained from T-PSA-3 + APC + PSA-3 Figure 6F).
  • Figures 7A-7H PSA polypeptides.
  • Figures 7A-7B precursor (SEQ ID NO:23) and mature (SEQ ID NO:24) PSA sequences.
  • Figures 7C7D precursor (SEQ ID NO:25) and mature (SEQ ID NO:26) PSA sequences comprising the PSA-3 (1-155) peptide.
  • Figures 7E-7F precursor (SEQ ID NO:27) and mature (SEQ ID NO:28) PSA sequences comprising the PSA-3 (Y154) peptide.
  • Figures 7G-7H precursor (SEQ ID NO:29) and mature (SEQ ID NO:30) PSA sequences comprising the PSA-3 (L155/Y154) peptide.
  • PSA-3 and PSA-3 agonist peptide sequences are underlined. Amino acid changes are shown in italics.
  • Nucleic acid or "polynucleotide” as used herein refers to purine- and pyrimidine- containing polymers of any length, either polyribonucleotides or polydeoxyribonucleotide or mixed polyribo-polydeoxyribonucleotides. This includes single-and double-stranded molecules, i.e., DNA-DNA, DNA-RNA and RNA-RNA hybrids, as well as “protein nucleic acids” (PNA) formed by conjugating bases to an amino acid backbone. This also includes nucleic acids containing modified bases.
  • PNA protein nucleic acids
  • Polynucleotides include naturally-occurring species or synthetic species formed from naturally-occurring subunits or their close homologs.
  • the term may also refer to moieties that function similarly to polynucleotides, but have nonnaturally-occurring portions.
  • polynucleotides may have altered sugar moieties or inter-sugar linkages. Exemplary among these are phosphorothioate and other sulfur containing species which are known in the art.
  • a “coding sequence” or a “protein-coding sequence” is a polynucleotide sequence capable of being transcribed into mRNA and/or capable of being translated into a polypeptide.
  • the boundaries of the coding sequence are typically determined by a translation start codon at the 5'-terminus and a translation stop codon at the 3'-terminus.
  • a “complement” or “complementary sequence” of a nucleic acid sequence as used herein refers to the antisense sequence that participates in Watson-Crick base-pairing with the original sequence.
  • a “probe” or “primer” refers to a nucleic acid or oligonucleotide that forms a hybrid structure with a sequence in a target region due to complementarily of at least one sequence in the probe or primer with a sequence in the target region.
  • vector refers to a nucleic acid molecule capable of replicating another nucleic acid to which it has been linked.
  • a vector for example, can be a plasmid, recombinant virus or transposon.
  • “Host” includes prokaryotes and eukaryotes. The term includes an organism or cell that is the recipient of a replicable vector.
  • isolated refers to nucleic or amino acid sequences that are at least 60% free, preferably 75% free, and most preferably 90% free from other components with which they are naturally associated.
  • proteins and “polypeptide” are synonymous.
  • Peptides are defined as fragments or portions of polypeptides, preferably fragments or portions having at least one functional activity (e.g., binding or antigenic activity) as the complete polypeptide sequence.
  • amino acid sequences may correspond to peptides or polypeptides.
  • antigenic refers to the ability of a molecule (e.g., a polypeptide or peptide) to bind to its specific antibody, or an antibody fragment, with sufficiently high affinity to form a detectable antigen-antibody complex.
  • sample refers to a biological sample, such as, for example, tissue or fluid isolated from an individual (including, without limitation, plasma, serum, cerebrospinal fluid, lymph, tears, saliva, milk, pus, and tissue exudates and secretions) or from in vitro cell culture constituents, as well as samples obtained from, for example, a laboratory procedure.
  • tissue or fluid isolated from an individual (including, without limitation, plasma, serum, cerebrospinal fluid, lymph, tears, saliva, milk, pus, and tissue exudates and secretions) or from in vitro cell culture constituents, as well as samples obtained from, for example, a laboratory procedure.
  • nucleic acids comprising nucleotide sequences (e.g., SEQ ID NO:20-SEQ ID NO:22) encoding one or more PSA-3 agonist peptides, PSA polypeptides comprising these peptides, or fragments or variants thereof.
  • nucleic acids may be single stranded or double stranded, and may include DNA or RNA molecules (e.g., DNA, DNA/DNA, RNA, or RNA/DNA) comprising 15, 18, 21, 24, 30 or more contiguous nucleotides, or complementary sequences thereof.
  • DNA or RNA molecules e.g., DNA, DNA/DNA, RNA, or RNA/DNA
  • nucleic acids comprising variant sequences maintain their desired function (e.g., expression, etc.).
  • this invention is directed to at least 24 contiguous nucleotides of a nucleic acid sequence encoding a PSA-3 agonist peptide.
  • polynucleotide variations are selected from the group consisting of at least one nucleotide deletion, substitution, including transition and transversion, insertion, or modification (e.g., via RNA or DNA analogs). Variations may occur at the 5' or 3' terminal positions of the reference nucleotide sequence or anywhere between those terminal positions, interspersed either individually among the nucleotides in the reference sequence or in one or more contiguous groups within the reference sequence. Variations of a polynucleotide sequence encoding a PSA-3 agonist peptide may create, nonsense, missense, or frameshift mutations in the coding sequence, and thereby alter the encoded peptide. However, variations may also create silent mutations in the coding sequence and leave the encoded peptide unchanged.
  • valine can be encoded by GTT, GTC, GTA, or GTG; leucine can be encoded by CTT, CTC, CTA, CTG, TTA, or TTG; serine can be encoded by TCT, TCC, TCA, TCG, AGT, or AGC; asparagine can be encoded by AAT or AAC; aspartic acid can be encoded by GAT or GAC; cysteine can be encoded by TGT or TGC; alanine can be encoded by GCT, GCC, GCA, or GCG; glutamine can be encoded by CAA or CAG; ty
  • Variant nucleic acids including DNA or RNA
  • hybridizations are a term of art which refers to the conditions of temperature and buffer concentration which permit hybridization of a particular nucleic acid to another nucleic acid in which the first nucleic acid may be perfectly complementary to the second, or the first and second may share some degree of complementarity which is less than perfect.
  • High stringency hybridization conditions are typically carried out at 65 to 68° C in 0.1 X SSC and 0.1 % SDS. Highly stringent conditions allow hybridization of nucleic acid molecules having about 95 to 100% sequence identity. Moderate stringency hybridization conditions are typically carried out at 50 to 65°C in 1 X SSC and 0.1 % SDS. Moderate stringency conditions allow hybridization of sequences having at least 80 to 95% nucleotide sequence identity. Low stringency hybridization conditions are typically carried out at 40 to 50° C in 6 X SSC and 0.1 % SDS. Low stringency hybridization conditions allow detection of specific hybridization of nucleic acid molecules having at least 50 to 80% nucleotide sequence identity.
  • the nucleic acid sequences of this invention may be derived from a variety of sources including genomic DNA, cDNA, synthetic DNA, synthetic RNA, or combinations thereof.
  • the sequences may be obtained in any of several ways.
  • the ⁇ polymerase chain reaction (PCR) method can be used to produce the nucleic acids of the invention, using either RNA (e.g., mRNA or synthetic RNA) or DNA (e.g., genomic DNA or synthetic DNA) as templates.
  • Primers used for PCR can be synthesized using the sequence information provided herein and can further be designed to introduce appropriate new restriction sites, if desirable, to facilitate incorporation into a given vector for recombinant expression.
  • nucleic acids described herein can be used in the methods of this invention for production of proteins or peptides, through incorporation (e.g., tranformation, transfection, or integration) into cells, tissues, or organisms.
  • DNA containing all or part of the coding sequence for a PSA-3 agonist peptide, or a fragment thereof, is incorporated into a vector for expression of the encoded polypeptide or peptide in suitable host cells.
  • the encoded polypeptide or peptide is capable of normal activity, such as antigenic or binding activity.
  • the nucleic acids of this invention also find use as primers and probes for, e.g., analysis of host cells containing PSA-3A vectors, or monitoring patients undergoing treatment with PSA-3A vectors or PSA-3A-modified host cells.
  • probes can be used in nucleic acid hybridization experiments, whereas primers can be used in PCR- based experiments.
  • the probes of this invention may be DNA or RNA.
  • the probes and primers of the invention may comprise all or a portion of the nucleotide sequence of the PSA-3 agonist nucleic acids (e.g., SEQ ID NO:20-SEQ ID NO:22), or a complementary sequence thereof, and may include promoter, enhancer elements, and additional PSA coding sequences.
  • one or more PSA-3 agonist peptides may be encoded by a viral or non- viral vector.
  • a number of viral vectors have been constructed, including polyoma, i.e., SV40 (Madzak et al., 1992, J. Gen. Virol, 73:15331536), adenovirus (Berkner, 1992, Curr. Top. Microbiol. Immunol, 158:39-6; Attorney Docket No.: 38163-0166
  • Baculovirus Autographa californica multinuclear polyhedrosis virus; AcMNPV
  • AcMNPV Baculovirus vectors are also known in the art, and may be obtained from commercial sources (e.g., PharMingen, San Diego, CA; Protein Sciences Corp., Meriden, CT; Stratagene, La Jolla, CA). Many human gene therapy protocols have been based on disabled murine retroviruses.
  • non-viral vectors can be transferred to hosts or host cells by well established methods, including chemical techniques such as calcium phosphate coprecipitation (Graham et al., 1973, Virology, 52:456-467; Pellicer et al., 1980, Science, 209:1414-1422), mechanical techniques, for example microinjection (Anderson et al, 1980, Proc. Natl. Acad. Sci. USA, 77:5399-5403; Gordon et al., 1980, Proc. Natl. Acad. Sci.
  • tecliniques include using a unique restriction endonuclease site that is naturally present or artificially inserted in the parental viral vector to insert the heterologous DNA.
  • Pox viruses useful in practicing the present invention include orthopox, suipox, avipox, and capripox virus.
  • Orthopox include vaccinia, ectromelia, and raccoon pox.
  • the preferred orthopox is vaccinia.
  • Avipox includes fowlpox, canary pox and pigeon pox.
  • the preferred avipox is fowlpox.
  • Capripox include goatpox and sheeppox.
  • a preferred suipox is swinepox. Examples of pox viral vectors for expression of PSA were provided in, for example, U.S. Patent No. 6,165,460 to Schlom, et al.
  • viral vectors that can be used include other DNA viruses such as herpes virus and adenoviruses, and RNA viruses such as retroviruses and polio.
  • vaccinia viral vectors may elicit a strong antibody response.
  • boosts with vaccinia vectors are possible, its repeated use may not be preferred in certain instances.
  • this sensitivity problem can be Attorney Docket No.: 38163-0166
  • the second and subsequent pox virus vectors are selected from the pox viruses from a different genus such as suipox, avipox, capripox or an orthopox immunogenically distinct from vaccinia.
  • the DNA donor vector contains the following elements: (i) a prokaryotic origin of replication, so that the vector may be amplified in a prokaryotic host; (ii) a gene encoding a marker which allows selection of prokaryotic host cells that contain the vector (e.g., a gene encoding antibiotic resistance); (iii) at least one DNA sequence encoding the PSA-3 agonist peptide, or a PSA polypeptide comprising this peptide, located adjacent to a transcriptional promoter capable of directing the expression of the sequence; and (iv) DNA sequences homologous to the region of the parent virus genome where the foreign gene(s) will be inserted, flanking the construct of element (iii).
  • Methods for constructing donor plasmids for the introduction of multiple foreign genes into pox virus are described in W091/19803, the techniques of which are incorporated herein by reference.
  • DNA fragments for construction of the donor vector can be obtained from genomic DNA or cloned DNA fragments.
  • the donor plasmids can be mono, di-, or multivalent (i.e., can contain one or more inserted foreign DNA sequences).
  • the donor vector preferably contains an additional gene that encodes a marker that will allow identification of recombinant viruses containing inserted foreign DNA.
  • marker genes can be used to permit the identification and isolation of recombinant viruses. These include genes that encode antibiotic or chemical resistance (e.g., see Spyropoulos et al, 1988, J.
  • the DNA gene sequence to be inserted into the virus can be placed into a donor plasmid, e.g., an E. coli plasmid construct, into which DNA homologous to a section of DNA such as that of the insertion site of the Attorney Docket No.: 38163-0166
  • poxvirus where the DNA is to be inserted has been inserted. Separately the DNA gene sequence to be inserted is ligated to a promoter. The promoter-gene linkage is positioned in the plasmid construct so that the promoter-gene linkage is flanked on both ends by DNA homologous to a DNA sequence flanking a region of pox DNA that is the desired insertion region. With a parental pox viral vector, a pox promoter is used. The resulting plasmid construct is then amplified by growth within E. coli bacteria and isolated.
  • the isolated plasmid containing the DNA gene sequence to be inserted is transfected into a cell culture, e.g., chick embryo fibroblasts, along with the parental virus, e.g., poxvirus.
  • a cell culture e.g., chick embryo fibroblasts
  • the parental virus e.g., poxvirus.
  • Recombination between homologous pox DNA in the plasmid and the viral genome respectively results in a recombinant poxvirus modified by the presence of the promoter- gene construct in its genome, at a site that does not affect virus viability.
  • the DNA sequence is inserted into a region (insertion region), in the virus that does not affect virus viability of the resultant recombinant virus.
  • a region insertion region
  • the skilled artisan can readily identify such regions in a virus by, for example, randomly testing segments of virus DNA for regions that allow recombinant formation without seriously affecting virus viability of the recombinant.
  • One region that can readily be used and is present in many viruses is the thymidine kinase (TK) gene.
  • the TK gene has been found in all pox virus genomes examined, including leporipoxvirus (Upton et al., 1986, J. Virology 60:920); shope fibromavirus; capripoxvirus (Gershon et al., 1989, J. Gen.
  • fowipox (Boyle et al., 1987, Virology 156:355); fowlpox (Schnitzlein et al., 1988, j. Virological Methods 20:341); fowlpox, quailpox; entomopox (Lytvyn et al., 1992, j. Gen. Virol. 73:3235- 3240).
  • hi vaccinia in addition to the TK region, other insertion regions include, for example, the Hindlll M fragment.
  • insertion regions include, for example, the BamHIl fragment (Jenkins et al., 1991, AIDS Research and Human Retroviruses 7:991-998) the ECORI-Hindlll fragment, EcoRV-Hindlll fragment, BamHl fragment and the Hindlll fragment set forth in ⁇ PO Application No. 0 Attorney Docket No.: 38163-0166
  • swinepox preferred insertion sites include the thymidine kinase gene region.
  • successful expression of the inserted gene by the modified poxvirus requires the presence of a promoter operably linked to the desired gene, i.e., in the proper relationship to the inserted gene.
  • the promoter must be placed so that it is located upstream from the gene to be expressed. Promoters are well known in the art and can readily be selected depending on the host and the cell type you wish to target. Preferably, in poxviruses, pox viral promoters are used, such as the vaccinia 7.5K, 40K or fowlpox promoters such as FPV CIA. Enhancer elements can also be used in combination to increase the level of expression. Furthermore, the use of inducible promoters, which are also well known in the art, may be advantageous.
  • Homologous recombination between donor plasmid DNA and viral DNA in an infected cell results in the formation of recombinant viruses that inco ⁇ orate the desired elements.
  • Appropriate host cells for in vivo recombination are generally eukaryotic cells that can be infected by the virus and transfected by the plasmid vector. Examples of such cells suitable for use with a pox virus are chick embryo fibroblasts, HuTK143 (human) cells, and CV-1 and BSC-40 (both monkey kidney) cells. Infection of cells with pox virus and transfection of these cells with plasmid vectors is accomplished by techniques standard in the art (Panicali and Paoletti, U.S. Pat. No. 4,603,112, W089/03429).
  • recombinant viral progeny can be identified by one of several techniques. For example, if the DNA donor vector is designed to insert foreign genes into the parent virus thymidine kinase (TK) gene, viruses containing integrated DNA will be TK- and can be selected on this basis (Mackett et al., 1982, Proc. Natl. Acad. Sci. USA 79:7415). Alternatively, co-integration of a gene encoding a marker or indicator gene with the foreign gene(s) of interest, as described above, can be used to identify recombinant progeny.
  • TK thymidine kinase
  • co-integration of a gene encoding a marker or indicator gene with the foreign gene(s) of interest as described above, can be used to identify recombinant progeny.
  • One preferred indicator gene is the E. coli lacZ gene.
  • Recombinant viruses expressing beta-galactosidase can be selected using a chromogemc substrate for the enzyme (Panicali et al., 1986, Gene 47:193). Once a recombinant virus has been identified, a variety of well-known methods can be used to assay the expression Attorney Docket No.: 38163-0166
  • PSA-3A the PSA sequence encoded by the inserted DNA fragment.
  • PSA-3A the PSA sequence encoded by the inserted DNA fragment.
  • black plaque assay an in situ enzyme immunoassay performed on viral plaques
  • Western blot analysis e.g., Western blot analysis
  • radioimmunoprecipitation RIPA
  • enzyme immunoassay EIA
  • a further aspect of this invention pertains to isolated PSA-3 agonist peptides (e.g., SEQ ID NO:3-SEQ ID NO:5), and PSA polypeptides comprising these peptides (e.g., SEQ ID NO:25-SEQ ID NO:30).
  • the peptides and polypeptides of this invention can be isolated, synthetic, or recombinant.
  • This invention encompasses PSA-3 agonist peptides and PSA polypeptides comprising these peptides, and fragments and functional equivalents thereof.
  • a functional equivalent is intended to include proteins which differ in amino acid sequence from the polypeptides or peptides of the invention, but where such differences result in a modified protein which performs at least one characteristic function of the polypeptide or peptide (e.g., binding or antigenic activity).
  • a functional equivalent of a polypeptide or peptide may have a variation such as a substitution, addition, deletion, or modification (e.g., phosphorylation, labeling, etc.) of an amino acid residue that is not directly involved in the function of the polypeptide or peptide.
  • polypeptides and peptides are modified so that they retain activity. Those residues shown to be essential for activity can be altered by replacing the essential amino acid with another, preferably similar amino acid residue (a conservative substitution) whose presence is shown to enhance, diminish, but not eliminate, or not effect function.
  • amino acid residues that are not essential for binding or other activity can be altered by being replaced by another amino acid whose incorporation may enhance, diminish, or not effect reactivity.
  • Polypeptide and peptide variants include mutants differing by the addition, deletion, or substitution of one or more amino acid residues. Also included are modified Attorney Docket No.: 38163-0166
  • Useful modifications may include phosphorylation, sulfation, reduction/alkylation (Tarr, 1986, Methods of Protein Microcharacterization, J. E. Silver, Ed., Humana Press, Clifton, NJ, pp. 155-194); acylation (Tarr, supra); chemical coupling (Mishell and Shiigi (Eds), 1980, Selected Methods in Cellular Immunology, W H Freeman, San Francisco, CA; U.S. Patent No. 4,939,239); and mild formalin treatment (Marsh, 1971, Int. Arch, of Allergy and Appl. Immunol. 41:199-215).
  • D-amino acids, non-natural amino acids, or non- amino acid analogs can be substituted or added to produce a modified polypeptide.
  • the polypeptides disclosed herein can be modified using polyethylene glycol (PEG) according to known methods (S.I. Wie et al., 1981, Int. Arch. Allergy Appl. Immunol. 64(1):8499) to produce a protein conjugated with PEG.
  • PEG polyethylene glycol
  • Modifications or sequence variations may occur at the amino- or carboxy-terminal positions of the reference polypeptide sequence or anywhere between those terminal positions, interspersed either individually among the amino acids in the reference sequence or in one or more contiguous groups within the reference sequence.
  • Polypeptides or peptides may also be modified with a label capable of providing a detectable signal, either directly or indirectly, including, but not limited to, radioisotope, fluorescent, and enzyme labels.
  • Fluorescent labels include, for example, CyTM3, CyTM5, Alexa, BODIPY, fluorescein (e.g., FluorX, DTAF, and FITC), rhodamine (e.g., TRITC), auramine, Texas Red, AMCA blue, and Lucifer Yellow.
  • Preferred isotope labels include 3 H, 14 C, 32 P, 35 S, 36 C1, 51 Cr, 57 Co, 58 Co, 59 Fe, 90 Y, 125 I, 131 I, and 186 Re.
  • Preferred enzyme labels include peroxidase, ⁇ -glucuronidase, ⁇ -D-glucosidase, ⁇ -Dgalactosidase, urease, glucose oxidase plus peroxidase, and alkaline phosphatase (see, e.g., U.S. Pat. Nos. 3,654,090; 3,850,752 and 4,016,043).
  • Enzymes can be conjugated by reaction with bridging molecules such as carbodiimides, diisocyanates, glutaraldehyde, and the like.
  • Enzyme labels can be detected visually, or measured by calorimetric, spectrophotometric, fluorospectrophotometric, amperometric, or gasometric techniques.
  • Other labeling systems such as avidin/biotin, Tyramide Signal Amplification (TSATM), are known in Attorney Docket No.: 38163-0166
  • polypeptide or peptide sequences may be identical to PSA-3 agonist peptides, or PSA polypeptides comprising these peptides, or may include up to a certain integer number of amino acid alterations.
  • Amino acid alterations are selected from the group consisting of at least one amino acid deletion, substitution, including conservative and non-conservative substitution, or insertion.
  • polypeptide and peptide variants may have conservative changes, wherein a substituted amino acid has similar structural or chemical properties, e.g., replacement of leucine with isoleucine. More infrequently, a variant may have nonconservative changes, e.g., replacement of a glycine with a tryptophan.
  • PSA-3 agonist peptides (e.g., SEQ ID NO:3-SEQ ID NO:5) contain V or Y at position 1; L or M at position 2; and V or I at position 10.
  • PSA-3 agonist peptides do not include D, E, or P at position 1; D or E at position 3; R, K, H or A at position 4; P at position 5; R, K or H at position 7; D, E, R, K or H at position 8; R, K or H at position 9; or L at position 10.
  • Substantial changes in function or immunogenicity can be made by selecting substitutions that are less conservative than those shown in the table, above.
  • non-conservative substitutions can be made which more significantly affect the structure of the polypeptide in the area of the alteration, for example, the alpha-helical, or beta-sheet structure; the charge or hydrophobicity of the molecule at the target site; or the bulk of the side chain.
  • substitutions which generally are expected to produce the greatest changes in the polypeptide's properties are those where 1) a hydrophilic residue, e.g., seryl or threonyl, is substituted for (or by) a hydrophobic residue, e.g., leucyl, isoleucyl, phenylalanyl, valyl, or alanyl; 2) a cysteine or proline is substituted for (or by) any other residue; 3) a residue having an electropositive side chain, e.g., lysyl, arginyl, or histidyl, is substituted for (or by) an electronegative residue, e.g., glutamyl or aspartyl; or 4) a residue having a bulky side chain, e.g., phenylalanine, is substituted for (or by) a residue that does not have a side chain, e.g., glycine.
  • a hydrophilic residue e.
  • Sequence tags e.g., epitope or protein tags
  • amino acids such as one or more lysines
  • epitope tags include c-myc, haemagglutinin (HA), polyhistidine (6X-HIS) (SEQ ID NO: 16), GLU-GLU, and DYKDDDDK (SEQ ID NO: 17; FLAG ® ) tags.
  • protein tags include glutathione-S- transferase (GST), green fluorescent protein (GFP), and maltose binding protein (MBP). Sequence tags can be used for peptide purification or localization. Lysines can be used to increase peptide solubility or to allow for biotinylation.
  • the instant invention also provides aptamers of peptides of the instant invention, hi a preferred embodiment, the invention provides aptamers of PSA-3 agonist peptides such as SEQ ID NO:3-SEQ ID NO:5.
  • the instant aptamers are peptide or nucleic acid molecules that are capable of binding to a protein or other molecule, or mimic the three dimensional structure of the active portion of the peptides of the invention. Aptamers may be prepared by any known method, including synthetic, recombinant, and purification methods (Nature 1996 Apr ll;380(6574):548-50).
  • PSA-3 agonist peptides e.g., SEQ ID Attorney Docket No. : 38163-0166
  • PSA polypeptides comprising these peptides (e.g., SEQ ID NO:25-SEQ ID NO:30), for use with this invention.
  • coding sequences may be cloned into any suitable vectors for expression in intact host cells or in cell-free translation systems by methods well known in the art (see Sambrook et al., 1989) and described herein. Alternately, peptides may be chemically synthesized by commercially available automated procedures.
  • polypeptides and peptides of this invention may be isolated from wild-type or mutant cells (e.g., human cells or cell lines), from heterologous organisms or cells (e.g., bacteria, yeast, insect, plant, and mammalian cells), or from cell- free translation systems (e.g., wheat germ, microsomal membrane, or bacterial extracts) in which a coding sequence has been introduced and expressed.
  • wild-type or mutant cells e.g., human cells or cell lines
  • heterologous organisms or cells e.g., bacteria, yeast, insect, plant, and mammalian cells
  • cell- free translation systems e.g., wheat germ, microsomal membrane, or bacterial extracts
  • DNA containing all or part of the coding sequence for PSA-3 agonist peptide (e.g., one or more of SEQ ID NO3-SEQ ID NO:5), or PSA polypeptide comprising this peptide, or variant thereof, is incorporated into a vector for expression of the encoded amino acid sequence in suitable host cells.
  • the encoded polypeptides, peptides, or their functional equivalents are capable of activity (i.e., binding or antigenic activity).
  • vectors including bacterial, yeast, and mammalian vectors, have been described for replication and/or expression in various host cells or cell-free systems, and may be used for vector-based therapies as well as for simple cloning or protein expression.
  • a vector e.g., expression vector
  • a nucleic acid encoding a PSA-3 agonist peptide, or PSA polypeptide comprising this peptide, as described herein, operably linked to at least one regulatory sequence.
  • regulatory sequence includes promoters, enhancers and other expression control elements (see, e.g., D.V. Goeddel, 1990, Methods Enzymol. 185:3-7).
  • Enhancer and other expression control sequences are described in Enhancers and Eukaryotic Gene Expression, l9 3, Cold Spring Harbor Press, Cold Spring Harbor, NY. It should be understood that the design of the vector may depend on such Attorney Docket No.: 38163-0166
  • Non-limiting examples of bacterial promoters include the ⁇ -lactamase (penicillinase) promoter; lactose promoter; tryptophan (trp) promoter; araBAD (arabinose) operon promoter; lambda-derived P 1 promoter and N gene ribosome binding site; and the hybrid tac promoter derived from sequences of the trp and lac UV5 promoters.
  • yeast promoters include the 3phosphoglycerate kinase promoter, glyceraldehyde-3-phosphate dehydrogenase (GAPDH) promoter, galactokinase (GAL1) promoter, galactoepimerase promoter, and alcohol dehydrogenase (ADHl) promoter.
  • Suitable promoters for mammalian cells include, without limitation, viral promoters, such as those from Simian Virus 40 (SV40), Rous sarcoma virus (RSV), adenovirus (ADV), and bovine papilloma virus (BPV).
  • SV40 Simian Virus 40
  • RSV Rous sarcoma virus
  • ADV adenovirus
  • BDV bovine papilloma virus
  • Preferred replication and inheritance systems include M 13, ColEl, SV40, baculovirus, lambda, adenovirus, CEN AIRS, 2 ⁇ m AIRS and the like. While vectors may replicate autonomously, they may also replicate by being inserted into the genome of the host cell, by methods well known in the art.
  • DNA sequences can be optimized, if desired, for more efficient expression in a given host organism or expression system.
  • codons can be altered to conform to the preferred codon usage in a given host cell or cell-free translation system using well- established techniques.
  • Codon usage data can be obtained from publicly-available sources, for example, the Codon Usage Database at hftp://www.kazusa. or.jp/codon/.
  • computer programs that translate amino acid sequence information into nucleotide sequence information in accordance with codon preferences are widely available.
  • sequences that cause amplification of the gene may also be desirable. These sequences are well known in the art. Furthermore, sequences that facilitate secretion of the recombinant product from cells, including, but not limited to, bacteria, yeast, and animal cells, such as secretory signal sequences and/or preprotein or proprotein sequences, may also be included. Such sequences are well described in the art.
  • Expression and cloning vectors will likely contain a selectable marker, a gene encoding a protein necessary for survival or growth of a host cell transformed with the vector. The presence of this gene ensures growth of only those host cells that express the inserts.
  • Typical selection genes encode proteins that 1) confer resistance to antibiotics or other toxic substances, e.g., ampicillin, neomycin, methotrexate, etc.; 2) complement auxotrophic deficiencies, or 3) supply critical nutrients not available from complex media, e.g., the gene encoding D-alanine racemase for Bacilli. Markers may be an inducible or non-inducible gene and will generally allow for positive selection.
  • Non-limiting examples of markers include the ampicillin resistance marker (i.e., beta-lactamase), tetracycline resistance marker, neomycin/kanamycin resistance marker (i.e., neomycin phosphotransferase), dihydrofolate reductase, glutamine synthetase, and the like.
  • ampicillin resistance marker i.e., beta-lactamase
  • tetracycline resistance marker i.e., tetracycline resistance marker
  • neomycin/kanamycin resistance marker i.e., neomycin phosphotransferase
  • dihydrofolate reductase i.e., glutamine synthetase
  • Suitable vectors for use with this invention include, but are not limited to, pUC, pBluescript (Stratagene), pET (Novagen, Inc., Madison, WI), and pREP (Invitrogen) plasmids.
  • Vectors can contain one or more replication and inheritance systems for cloning or expression, one or more markers for selection in the host, e.g., antibiotic resistance, and one or more expression cassettes.
  • the inserted coding sequences can be synthesized by standard methods, isolated from natural sources, or prepared as hybrids. Ligation of the coding sequences to transcriptional regulatory elements (e.g., promoters, enhancers, and/or insulators) and/or to other amino acid encoding sequences can be carried out using established methods.
  • Suitable cell-free expression systems for use with this invention include, without limitation, rabbit reticulocyte lysate, wheat germ extract, canine pancreatic microsomal membranes, E. coli S30 extract, and coupled Attorney Docket No.
  • telomeres telomeres
  • suitable host cells include bacteria, archea, insect, fungi
  • yeast e.g., yeast
  • animal cells e.g., mammalian, especially human.
  • Escherichia coli Bacillus subtilis, Saccharomyces cerevisiae, SF9 cells, C129 cells, 293 cells, Neurospora, and immortalized mammalian myeloid and lymphoid cell lines. Techniques for the propagation of mammalian cells in culture are well-known (see, Jakoby and Pastan (eds), 1979, Cell Culture. Methods in Enzymology, volume 58, Academic Press, Inc., Harcourt Brace Jovanovich, NY).
  • mammalian host cell lines examples include VERO and HeLa cells, CHO cells, and WI38, BHK, and COS cell lines, although it will be appreciated by the skilled practitioner that other cell lines may be used, e.g., to provide higher expression desirable glycosylation patterns, or other features.
  • Host cells can be transformed, transfected, or infected as appropriate by any suitable method including electroporation, calcium chloride-, lithium chloride-, lithium acetate/polyethylene glycol-, calcium phosphate-, DEAEdextran-, liposome-mediated DNA uptake, spheroplasting, injection, microinjection, microprojectile bombardment, phage infection, viral infection, or other established methods.
  • vectors containing the nucleic acids of interest can be transcribed in vitro, and the resulting RNA introduced into the host cell by well-known methods, e.g., by injection (see, Kubo et al., 1988, FEBS Letts. 241:119).
  • nucleic acids into which have been introduced nucleic acids described above are meant to also include the progeny of such cells.
  • Nucleic acids encoding the PSA-3 agonist peptides, polypeptides comprising these peptides, or variants or fragments thereof can be produced in large quantities by replication in a suitable host cell.
  • Synthetic nucleic acid fragments comprising at least 15 contiguous bases coding for a desired peptide or polypeptide can be incorporated into recombinant nucleic acid constructs, e.g., DNA constructs, capable of introduction into and replication in a prokaryotic or eukaryotic cell.
  • the most commonly used prokaryotic hosts are strains of Escherichia coli, although other prokaryotes, such as Bacillus subtilis Attorney Docket No.: 38163-0166
  • nucleic acids of the invention may also be used.
  • mammalian or other eukaryotic host cells such as those of yeast, filamentous fungi, plant, insect, or amphibian or avian species, may also be useful for isolation of the nucleic acids of the invention.
  • the purification of nucleic acids produced by the methods of this invention is described, for example, in Sambrook et al., 1989; F.M. Ausubel et al., 1992, Current Protocols in Molecular Biology, J. Wiley and Sons, New York, NY.
  • nucleic acids encoding the peptides or polypeptides of this invention can also be produced by chemical synthesis, e.g., by the phosphoramidite method described by Beaucage et al., 1981, Tetra. Zetto.22:1859-1862, or the triester method according to Matteucci et al., 1981, J. Am. Chem. Soc, 103:3185, and can performed on commercial, automated oligonucleotide synthesizers.
  • a double-stranded fragment may be obtained from the single-stranded product of chemical synthesis either by synthesizing the complementary strand and annealing the strands together under appropriate conditions or by adding the complementary strand using DNA polymerase with an appropriate primer sequence.
  • PSA-3 agonist peptides can be chemically synthesized by commercially available automated procedures, including, without limitation, exclusive solid phase synthesis, partial solid phase methods, fragment condensation, classical solution synthesis.
  • recombinant and synthetic methods of peptide production can be combined to produce semi-synthetic peptides.
  • the peptides of the invention are preferably prepared by solid phase peptide synthesis as described by Merrifield, 1963, J. Am. Chem. Soc. 85:2149; 1997. In one embodiment, synthesis is carried out with amino acids that are protected at the alphaamino terminus.
  • Trifunctional amino acids with labile side-chains are also protected with suitable groups to prevent undesired chemical reactions from occurring during the assembly of the peptides.
  • the alpha-amino protecting group is selectively removed to allow subsequent reaction to take place at the amino-terminus. The conditions for the removal of the alpha-amino protecting group do not remove the side-chain protecting groups.
  • alpha-amino protecting groups are those known to be useful in the art of stepwise peptide synthesis, included are acyl type protecting groups, e.g., formyl, trifluoroacetyl, acetyl, aromatic urethane type protecting groups, e.g., benzyloxycarbonyl Attorney Docket No.: 38163-0166
  • Boc substituted benzyloxycarbonyl and 9-fluorenylmethyloxycarbonyl
  • aliphatic urethane protecting groups e.g., t-butyloxycarbonyl (Boc)
  • alkyl type protecting groups e.g., benzyl, triphenylmethyl.
  • the preferred protecting group is Boc.
  • the side-chain protecting groups for Tyr include tetra hydropyranyl, tert-butyl, trityl, benzyl, Cbz, 4-Br-Cbz and 2,6dichlorobenzyl.
  • the preferred side-chain protecting group for Tyr is 2,6dichlorobenzyl.
  • the side-chain protecting groups for Asp include benzyl, 2,6-dichlorobenzyl, methyl, ethyl, and cyclohexyl.
  • the preferred side-chain protecting group for Asp is cyclohexyl.
  • the side- chain protecting groups for Thr and Ser include acetyl, benzoyl, trityl, tetrahydropyranyl, - benzyl, 2,6dichlorobenzyl, and Cbz.
  • the preferred protecting group for Thr and Ser is benzyl.
  • the side-chain protecting groups for Arg include nitro, Tos, Cbz, adamantyloxycarbonyl, and Boc.
  • the preferred protecting group for Arg is Tos.
  • the side- chain amino group of Lys can be protected with Cbz, 2-Cl-Cbz, Tos, or Boc.
  • the 2-C1- Cbz group is the preferred protecting group for Lys.
  • the side-chain protecting groups selected must remain intact during coupling and not be removed during the deprotection of the amino-terminus protecting group or during coupling conditions.
  • the side-chain protecting groups must also be removable upon the completion of synthesis, using reaction conditions that will not alter the finished peptide.
  • Solid phase synthesis is usually carried out from the carboxyterminus by coupling the alpha-amino protected (side-chain protected) amino acid to a suitable solid support.
  • An ester linkage is formed when the attachment is made to a chloromethyl or hydroxymethyl resin, and the resulting peptide will have a free carboxyl group at the C-terminus.
  • a benzhydrylamine or p-methylbenzhydrylamine resin is used, an amide bond is formed and the resulting peptide will have a carboxamide group at the C- terminus.
  • These resins are commercially available, and their preparation has described by Stewart et al, 1984, Solid Phase Peptide Synthesis (2nd Edition), Pierce Chemical Co., Rockford, IL.
  • DCC dicyclohexylcarbodiimide
  • N,N'-diisopropyl-carbodiimide N,N'-diisopropyl-carbodiimide
  • carbonyldiimidazole carbonyldiimidazole
  • TFA trifluoroacetic acid
  • Metal methionine
  • Various activating agents can be used for the coupling reactions including DCC,N,N'-diisopropyl-carbodiimide, benzotriazol- 1 -yl-oxy-tris-(dimethylamino) phosphonium hexa-fluorophosphate (BOP) and DCC-hydroxybenzotriazole (HOBt).
  • BOP benzotriazol- 1 -yl-oxy-tris-(dimethylamino) phosphonium hexa-fluorophosphate
  • HOBt DCC-hydroxybenzotriazole
  • the coupling reaction is repeated.
  • the coupling reactions can be performed automatically with commercially available instruments.
  • the peptide-resin is cleaved with a reagent such as liquid HF for 1-2 hours at 0°C, which cleaves the peptide from the resin and removes all side-chain protecting groups.
  • a scavenger such as anisole is usually used with the liquid HF to prevent cations formed during the cleavage from alkylating the amino acid residues present in the peptide.
  • the peptide-resin can be deprotected with 5 TFA/dithioethane prior to cleavage if desired.
  • Cyclization is achieved on the solid support using various activating agents including DCC, DCC/HOBt, or BOP.
  • the HF reaction is carried out on the cyclized peptide-resin as described above.
  • Methods for polypeptide and peptide purification are well-known in the art, including, without limitation, preparative disc-gel electrophoresis, isoelectric focusing, Attorney Docket No.: 38163-0166
  • the polypeptide or peptide in a recombinant system in which the protein contains an additional sequence (e.g., epitope or protein) tag that facilitates purification (see above).
  • the coding sequence of a polypeptide or peptide can be cloned into a vector that creates a fusion with a sequence tag of interest.
  • Suitable vectors include, without limitation, pRSET (invitrogen Corp., San Diego, CA), pGEX (Amersham- Pharmacia Biotech, Inc., Piscataway, NJ), pEGFP (CLONTECH Laboratories, Inc., Palo Alto, CA), and pMALTM (New England BioLabs (NEB), h e, Beverly, MA) plasmids.
  • the epitope, or protein tagged polypeptide or peptide can be purified from a crude lysate of the translation system or host cell by chromatography on an appropriate solid-phase matrix, hi some cases, it may be preferable to remove the epitope or protein tag (i.e., via protease cleavage) following purification.
  • antibodies produced against a protein or peptide can be used as purification reagents. Other purification methods are also possible. Antibodies
  • Another aspect of the invention pertains to antibodies directed to a PSA-3 agonist peptide (e.g., SEQ ID NO:3-SEQ ID NO:5), a PSA polypeptide comprising this peptide, or fragments or variants thereof.
  • the invention provides polyclonal and monoclonal antibodies.
  • the antibodies may be elicited in an animal host (e.g., rabbit, goat, mouse, or other nonhuman mammal) by immunization with disorder-associated immunogenic components.
  • Antibodies may also be elicited by in vitro immunization (sensitization) of immune cells.
  • the immunogenic components used to elicit the production of antibodies may be isolated from cells or chemically synthesized.
  • the antibodies may also be produced in recombinant systems programmed with appropriate antibody-encoding DNA. Alternatively, the antibodies may be constructed by biochemical reconstitution of purified heavy and light chains.
  • the antibodies include hybrid antibodies, chimeric antibodies, and univalent antibodies. Also included are Fab fragments, including Fab 1 and Fab(ab) 2 fragments of antibodies.
  • An isolated PSA-3 agonist peptide, a PSA polypeptide comprising this peptide, or fragment or variant thereof, can be used as an immunogen to generate antibodies using Attorney Docket No.: 38163-0166
  • PSA polypeptides can be used or, alternatively, the invention provides antigenic peptide portions of these polypeptides for use as immunogens.
  • An antigenic peptide of the invention comprises a sufficient number of contiguous amino acid residues of the amino acid sequence, or a variant thereof, to encompass an epitope of a PSA polypeptide such that an antibody raised against the peptide forms a specific immune complex with the peptide or polypeptide.
  • at least 5 contiguous amino acids are sufficient to define an epitope.
  • a PSA-3 agonist epitope may comprise at least 8 contiguous amino acids.
  • An appropriate immunogenic preparation can contain, for example, 1) recombinantly produced PSA-3 agonist peptides, or PSA polypeptides comprising these peptides; 2) chemically synthesized PSA-3 agonist peptides or PSA polypeptides comprising these peptides, or 3) fragments or variants of (l)-(2).
  • the preparation can further include an adjuvant, such as Freund's complete or incomplete adjuvant, or similar immunostimulatory agent. A number of adjuvants are known and used by those skilled in the art.
  • Non-limiting examples of adjuvants include incomplete Freund's adjuvant, and surface-active substances such as lysolecithin, pluronic polyols, polyanions, peptides, oil emulsions, keyhole limpet hemocyanin, and dinitrophenol. Further examples of adjuvants include stearyl tyrosine (A. Nixon-George et al., 1990, J Immunol. 144:4798-4802; Paoletti, et al, 1997, J. Infect. Diseases 175:1237-9; U.S. Pat. No. 4,258,029 to Moloney et al.; U.S. Pat. No.
  • N-acetyl-muramyl-Lthreonyl-D- isoglutamine thr-MDP
  • N-acetyl-nor-muramyl-L-alanyl-Disoglutamine CGP 11637, referred to as nor-MDP
  • N-acetylmuramylLalanyl-D-isoglutaminyl-L-alanine-2-(r- 2'-dipalmitoyl-sn-glycero-3 hydroxyphosphoryl-oxy)-ethylamine CGP 19835A, referred to as MTP-PE
  • One particular adjuvant comprises 5% (wt/vol) squalene, 2.5% Pluronic L121 polymer and 0.2%) polysorbate in phosphate buffered saline (Kwak et al., 1992, New Eng. J. Med. 327:1209-1215). More examples of adjuvants are listed herein below.
  • the effectiveness of an adjuvant may be determined by measuring the amount of antibodies directed against the immunogenic peptide.
  • the immunogen can be conjugated to a carrier protein, if desired, to increase immunogenicity, particularly, if a small peptide is used. Commonly used carriers that are Attorney Docket No. : 38163-0166
  • peptides routinely used chemically coupled to peptides include serum albumins, e.g., bovine, sheep, goat, or fish serum albumin, thyroglobulin, and keyhole limpet hemocyanin.
  • the coupled immunogencarrier is then used to immunize a recipient animal (e.g., mouse, rat, sheep, goat, or rabbit).
  • the antibody titer in the immunized animal can be monitored over time by standard techniques, such as with an enzyme linked immunosorbent assay (ELISA) using immobilized PSA-3 agonist peptide, or a PSA polypeptide comprising this peptide.
  • ELISA enzyme linked immunosorbent assay
  • the antibody molecules can be isolated from the mammal (e.g., from the blood) and further purified by well-known tecliniques, such as protein A chromatography to obtain the IgG fraction.
  • tecliniques such as protein A chromatography
  • antibody-producing cells can be obtained from the animal subject and used to prepare monoclonal antibodies by standard techniques, such as the hybridoma technique (see Kohler and Milstein, 1975, Nature 256:495-497; Brown et al., 1981, J. Immunol. 127:539-46; Brown et al., 1980, J. Biol Chem.
  • an immortal cell line typically a myeloma
  • lymphocytes typically splenocytes
  • a PSA-3 agonist immunogen e.g., peptide or polypeptide
  • the culture supernatants of the resulting hybridoma cells are screened to identify a hybridoma producing a monoclonal antibody that binds a PSA-3 agonist peptide or PSA polypeptide comprising this peptide.
  • the immortal cell line (e.g., a myeloma cell line) is derived from the same mammalian species as the lymphocytes.
  • murine hybridomas can be made by fusing lymphocytes from a mouse immunized with an immunogenic preparation of this invention with an immortalized mouse cell line.
  • Preferred immortal cell lines are mouse myeloma cell lines that are sensitive to culture medium containing hypoxanthine, aminopterin, and thymidine (HAT medium).
  • myeloma cell lines can be used as a fusion partner according to standard techniques, e.g., the P3-NSl/l-Ago-l, P3-x63-Ag8.653, or Sp2/O-Agl4 myeloma lines. These myeloma lines are available from ATCC (American Type Culture Collection, Manassas, VA). Typically, HAT-sensitive mouse myeloma cells are fused to mouse splenocytes using polyethylene glycol (PEG).
  • PEG polyethylene glycol
  • Hybridoma cells producing a monoclonal antibody of the invention are detected by screening the hybridoma culture supematants for antibodies that bind the PSA-3 agonist peptide, e.g., using a standard ELISA assay.
  • a monoclonal antibody can be identified and isolated by screening a recombinant combinatorial immunoglobulin library (e.g., an antibody phage display library) with the corresponding PSA-3 agonist peptide to thereby isolate immunoglobulin library members that bind these molecules.
  • Kits for generating and screening phage display libraries are commercially available (e.g., the Pharmacia Recombinant Phage Antibody System, Catalog No. 279400- 01; and the Stratagene SurfZAPTM Phage Display Kit, Catalog No. 240612). Examples of methods and reagents particularly amenable for use in generating and screening antibody display library can be found in, for example, A. Blume U.S.
  • recombinant antibodies to a PSA-3 agonist peptide, or PSA polypeptide comprising this peptide can be made using standard recombinant DNA techniques.
  • chimeric and humanized monoclonal antibodies that comprise both human and non-human portions can be produced.
  • Exemplary methods for producing chimeric and humanized monoclonal antibodies are described in, for example, Robinson et al. international Application No. PCT/US86/02269; Akira, et al. European Patent Application 184,187; Taniguchi, M., European Patent Application 171,496; Morrison et al. European Patent Application 173,494; Neuberger et al. PCT International Publication No.
  • An antibody against a PSA-3 agonist peptide or a PSA polypeptide comprising this peptide can be used to isolate the corresponding molecule by standard techniques, such as affinity chromatography or immunoprecipitation.
  • antibodies can facilitate the purification of recombinantly produced PSA polypeptides or PSA-3 agonist peptides from host cells, h addition, an antibody that binds to a PSA-3 agonist peptide can be used to detect the corresponding peptide or a PSA polypeptide comprising this peptide (e.g., in a cellular lysate or cell supernatant) in order to evaluate patterns or levels of protein expression.
  • Such antibodies can also be used as diagnostics to monitor PSA polypeptide or PSA-3 agonist peptide levels in tissue as part Attorney Docket No.: 38163-0166
  • This invention provides methods of screening for drugs using PSA-3 agonist peptides (e.g., SEQ ID NO:3-SEQ ID NO:5), polypeptides comprising these peptides (e.g., SEQ ID NO:25-SEQ ID NO:30), or fragments or variants thereof, in competitive binding assays, according to methods well-known in the art.
  • PSA-3 agonist peptides e.g., SEQ ID NO:3-SEQ ID NO:5
  • polypeptides e.g., SEQ ID NO:25-SEQ ID NO:30
  • fragments or variants thereof in competitive binding assays, according to methods well-known in the art.
  • competitive drug screening assays can be employed using complexes comprising PSA-3 agonist peptides and HLA-A2 molecules, and screening for test agents that disrupt, enhance, or otherwise alter the peptide-HLA complex.
  • Agents that disrupt the peptide-HLA complex may serve as analogs that mimic the function of
  • Test agents may encompass numerous chemical classes, though typically they are organic molecules, e.g., small molecules. Preferably, test agents have a molecular weight of less than 5000 daltons, more preferably, test agents have a molecular weight of more than 50 and less than 2,500 daltons.
  • Such test agents can comprise functional groups necessary for structural interaction with proteins, particularly hydrogen bonding, and typically include at least an amine, carbonyl, hydroxyl or carboxyl group, preferably at least two of the functional chemical groups.
  • Useful test agents often comprise cyclical carbon or heterocyclic structures and/or aromatic or polyaromatic structures substituted with one or more of the above functional groups.
  • test agents can also comprise biomolecules including peptides, saccharides, fatty acids, steroids, purines, pyrimidines, derivatives, structural analogs, or combinations thereof.
  • Test agents may include, for example, 1) peptides such as soluble peptides, including Ig-tailed fusion peptides and members of random peptide libraries (see, e.g., Lam et al., 1991, Nature 354:82-84; Houghten et al., 1991, N ⁇ twre 354:84-86) and combinatorial chemistry-derived molecular 5 libraries made of D- and/or L-configuration amino acids; 2) phosphopeptides (e.g., members of random and partially degenerate, directed phosphopeptide libraries, see, e.g., Songyang et al, 1993, Cell 72:767-778); 3) antibodies (e.g., polyclonal, monoclonal, humanized, anti-idiotypic, chimeric, and single Attorney
  • Test agents can be obtained from a wide variety of sources including libraries of synthetic or natural compounds.
  • Synthetic compound libraries are commercially available from, for example, Maybridge Chemical Co. (Trevillet, Cornwall, UK), Comgenex (Princeton, NJ), Brandon Associates (Merrimack, NH), and Microsource (New Milford, CT).
  • a rare chemical library is available from Aldrich Chemical Company, Inc. (Milwaukee, WI).
  • Natural compound libraries comprising bacterial, fungal, plant or animal extracts are available from, for example, Pan Laboratories (Bothell, WA). h addition, numerous means are available for random and directed synthesis of a wide variety of organic compounds and biomolecules, including expression of randomized oligonucleotides.
  • libraries of natural compounds in the form of bacterial, fungal, plant and animal extracts can be readily produced.
  • Methods for the synthesis of molecular libraries are readily available (see, e.g., DeWitt et al., 1993, Proc. Natl. Acad. Sci. USA 90:6909; Erb et al., 1994, Proc. Natl. Acad. Sci. USA 91:11422; Zuckermann et al., 1994, J. Med. Chem. 37:2678; Cho et al, 1993, Science 261:1303; Carell et al., 1994, Angew. Chem. Int. Ed. Engl 33:2059; Carell et al., 1994, Angew. Chem.
  • Non-limiting examples of small molecules, small molecule libraries, combinatorial libraries, and screening methods are described in B. Seligmann, 1995, "Synthesis,
  • Libraries may be screened in solution (e.g., Houghten, 1992, Biotechniques 13:412-421), or on beads (Lam, 1991, Nature 354:82-84), chips (Fodor, 1993, Nature 364:555-556), bacteria or spores (Ladner U.S. Pat. No. 5,223,409), plasmids (Cull et al., 1992, Proc. Natl. Acad. Sci. USA 89:1865-1869), or on phage (Scott and Smith, 1990, Science 249:386-390; Devlin, 1990, Science 249:404-406; Cwirla et al., 1990, Proc. Natl Acad. Sci. USA 97:6378-6382; Felici, 1991, J. Mol. Biol. 222:301-310; Ladner, supra).
  • a PSA-3 agonist peptide, PSA polypeptide comprising this peptide, or variant or fragment thereof may be joined to a label, where the label can directly or indirectly provide a detectable signal.
  • Various labels include radioisotopes, fluorescers, chemiluminescers, enzymes, specific binding molecules, particles, e.g., magnetic particles, and the like.
  • Specific binding molecules include pairs, such as biotin and streptavidin, digoxin and antidigoxin, etc.
  • the complementary member would normally be labeled with a molecule that provides for detection, in accordance with known procedures.
  • reagents may be included in the screening assay. These include reagents like salts, neutral proteins, e.g., albumin, detergents, etc., that are used to facilitate optimal protein-protein binding and/or reduce non-specific or background interactions. Reagents that improve the efficiency of the assay, such as protease inhibitors, nuclease inhibitors, anti-microbial agents, etc., may be used. The components are added in any order that produces the requisite binding. Incubations are performed at any temperature that facilitates optimal activity, typically between 4 and 40°C. Incubation periods are selected for optimum activity, but may also be optimized to facilitate rapid high-throughput screening.
  • a plurality of assay mixtures is run in parallel with different agent concentrations to obtain a differential response to these concentrations.
  • one of these concentrations serves as a negative control, i.e., at zero concentration or below the level of detection.
  • a PSA-3 agonist peptide PSA polypeptide comprising this peptide, or fragment or variant thereof
  • a fusion protein comprising a PSA-3 agonist peptide and an affinity tag can be produced.
  • a fusion protein comprising a PSA-3 agonist peptide and FLAGS tag is adsorbed onto anti-FLAG® tag conjugated beads or microtiter plates.
  • Labeled (e.g., radiolabeled) test agents are added to the coated beads under conditions to allow complex formation (e.g., at physiological conditions for salt and pH). Following incubation, the coated beads are washed to remove any unbound test agents, and the amount of immobilized radiolabel is determined. Alternatively, the complex is dissociated and the radiolabel present in the supernatant is determined. In another approach, the beads are analyzed by SIDS-PAGE to identify the bound agents.
  • the invention further provides methods of rational drug design employing PSA-3 agonist peptides, polypeptides comprising these peptides, antibodies that bind to these peptides, or portions or functional equivalents thereof.
  • the goal of rational drug design is to produce structural analogs, e.g., mimetics, of biologically active polypeptides of interest or of small molecules with which they interact, hi turn, these analogs can be used to fashion drugs which are, for example, more active or stable forms of the PSA-3 agonist Attorney Docket No.: 38163-0166
  • the three-dimensional structure of a PSA-3 agonist peptide, or polypeptide comprising this peptide is determined by x-ray crystallography, computer modeling, or a combination thereof. Useful information regarding the structure of a peptide or polypeptide can also be gained by computer modeling based on the structure of homologous proteins.
  • PSA-3 agonist peptides, polypeptides comprising these peptides, or fragments thereof can be analyzed by alanine scans (Wells, 1991, Methods in Enzymol, 202:390-4.11). In this technique, each amino acid residue in a polypeptide or peptide is replaced by alanine, and its effect on the activity of the polypeptide is determined.
  • an antibody specific to a PSA-3 agonist peptide can be isolated, selected by a functional assay, and then analyzed to solve its crystal structure, hi principle, this approach can yield a pharmacore upon which subsequent drug design can be based.
  • anti-ids anti-idiotypic antibodies
  • the binding site of the anti-ids is predicted to be an analog of the corresponding PSA-3 agonist peptide.
  • the anti-id can then be used to identify and isolate peptides from banks of chemically or biologically produced banks of peptides. Selected peptides can subsequently be used as pharmacores.
  • Non-limiting examples of methods and computer tools for drug design are described in R. Cramer et al., 1974, J. Med. Chem. 17:533; H. Kubinyi (ed) 1993, 3D QSAR in Drug Design, Theory, Methods, and Applications, ESCOM, Leiden, Holland; P. Dean (ed) 1995, Molecular Similarity in Drug Design, K. Kim "Comparative molecular field analysis (ComFA)” p. 291-324, Chapman & Hill, London, UK; Y. et al., 1993, J. Comp.-Aid. Mol. Des. 7:83102; G. Lauri and P. A. Bartlett, 1994, J. Comp.-Aid. Mol. Des.
  • cells and animals that carry PSA3 agonist peptides, PSA polypeptides comprising these peptides, or fragments or variants thereof can be used as model systems to study and test for agents that have potential as therapeutic compounds.
  • a test agent is administered to animals or applied to the cells, the phenotype of the animals/cells can be determined.
  • cytotoxic T cells can be used to screen for compounds that enhance the ability of the PSA-3 agonist peptide to create a cytotoxic T cell response, hi this type of screen, cytotoxic T cells are incubated with a selected epitope, for example, in a microtiter plate.
  • the agent to be tested e.g.
  • a drug is then added to the well and the growth of the T cells is measured. T cell expansion indicates that the test agent enhances the T cell response. Test agents that enhanced T cell response are then subjected to further evaluation. hi accordance with these methods, one may design drugs that result in, for example, enhanced immunoreactivity to PSA.
  • PSA-3 agonist peptides By virtue of the availability of nucleotide sequences encoding PSA-3 agonist peptides, sufficient amounts of these peptides, or polypeptides comprising these peptides, may be produced to perform such analytical studies as x-ray crystallography. In addition, the knowledge of the PSA-3 agonist peptide sequences will guide those employing computer-modeling techniques in place of, or in addition to x-ray crystallography.
  • antibodies which specifically bind to a PSA-3 agonist peptide e.g., SEQ ID NO:3-SEQ ID NO:5
  • a PSA polypeptide comprising this peptide e.g., SEQ ID NO:25-SEQ ID NO:30
  • the antibodies useful for diagnostic purposes may be prepared in the same manner as those disclosed above.
  • Antibodies may be raised to a full- length PSA-3 agonist peptide, or a PSA polypeptide comprising this peptide. Alternatively, the antibodies may be raised to portions or variants of this peptide or polypeptide.
  • Diagnostic assays for PSA-3 agonist peptides, or PSA polypeptides comprising these peptides include methods that utilize the antibody and a label to detect the peptides or polypeptides in biological samples (e.g., human body fluids, cells, tissues, or extracts of Attorney Docket No.: 38163-0166
  • the antibodies may be used with or without modification, and may be labeled by joining them, either covalently or non-covalently, with a reporter molecule.
  • reporter molecules A wide variety of reporter molecules that are known in the art may be used, several of which are described herein. Many immunoassay formats are known in the art, and the particular format used is determined by the desired application.
  • An immunoassay can use, for example, a monoclonal antibody directed against a single disease-associated epitope, a combination of monoclonal antibodies directed against different epitopes of a single disease-associated antigenic component, monoclonal antibodies directed towards epitopes of different disease-associated antigens, polyclonal antibodies directed towards the same disease- associated antigen, or polyclonal antibodies directed towards different disease-associated antigens. Protocols can also, for example, use solid supports, or may involve immunoprecipitation. Typically, immunoassays use either a labeled antibody or a labeled antigenic component (i.e., to compete with the antigen in the sample for binding to the antibody). Exemplary labels are described in the sections shown above.
  • the amount of antibody-antigen association may be quantified by various methods; photometric means are prefened. Levels of the polypeptide or peptide in the post-treatment sample and in the pretreatment (negative control) sample are compared. The difference between pre-treatment and post- treatment values establishes the parameters for monitoring levels during treatment protocols.
  • Kits suitable for antibody-based diagnostic applications typically include one or more of the following components: Attorney Docket No.: 38163-0166
  • Antibodies The antibodies may be pre-labeled. Alternatively, the antibody may be unlabeled and the ingredients for labeling may be included in the kit in separate containers, or a secondary, labeled antibody is provided. Antibodies may be monoclonal or polyclonal, and may be directed to PSA-3 agonist peptides, or PSA polypeptides comprising these peptides, or variants or fragments thereof;
  • the kit may also contain other suitably packaged reagents and materials needed for the particular immunoassay protocol, including solid- phase matrices, if applicable, and standards.
  • kits referred to above may include instructions for conducting the test. Furthermore, in preferred embodiments, the diagnostic kits are adaptable to high- throughput and/or automated operation.
  • PSA-3 agonist nucleic acids e.g., SEQ ID NO:20-SEQ ID NO:22
  • the invention therefore provides methods for detecting levels or sequences of PSA-3 agonist nucleic acids in a sample, such as in a biological sample (e.g., human body fluids, cells, tissues, or extracts of cells or tissues).
  • PSA-3 agonist polynucleotide sequences can be detected by DNA-DNA or DNARNA hybridization, or by amplification, using probes or primers comprising at least a portion of a disclosed polynucleotide, or a sequence complementary thereto.
  • PSA-3 agonist oligonucleotides or oligomers i.e. primers
  • nucleic acid amplification-based assays e.g., PCR assays
  • PSA-3 oligomers, i.e., probes can be used in nucleic acid hybridization-based assays (e.g., Southern, dot, or slot blots) to detect cells or other biological samples containing PSA-3 agonist DNA or RNA.
  • nucleic acids useful as probes or primers in diagnostic methods include oligonucleotides at least 15 contiguous nucleotides in length, more preferably at least 18, 21, 24, or 30, contiguous nucleotides in length, that hybridize specifically with PSA-3 agonist nucleic acids.
  • labeled probes can be produced by oligo-labeling, nick translation, end-labeling, or PCR amplification using a labeled nucleotide.
  • PSA-3 agonist polynucleotide sequences, or any portions or fragments thereof may be cloned into a vector for the production of an mRNA probe.
  • Such vectors are known in the art, are commercially available, and may be used to synthesize RNA probes in vitro by addition of an appropriate RNA polymerase, such as T7, T3, or SP(6) and labeled nucleotides.
  • reporter molecules or labels which may be used include radionucleotides (e.g., 32P, 3H, and 35S), enzymes, fluorescent (e.g., rhodamine, fluorescein, and CyTM3, CyTM5), chemiluminescent, or chromo genie agents, and other labels (e.g., DNP, digoxigenin, and biotin) such as substrates, cofactors, inhibitors, magnetic particles, and the like.
  • radionucleotides e.g., 32P, 3H, and 35S
  • enzymes e.g., fluorescent (e.g., rhodamine, fluorescein, and CyTM3, CyTM5)
  • chemiluminescent chemiluminescent
  • chromo genie agents e.g., DNP, digoxigenin, and biotin
  • a sample to be analyzed such as, for example, a tissue sample (e.g., hair or buccal cavity) or body fluid sample (e.g., blood, saliva, or urine), may be contacted directly with the nucleic acid probes. Alternatively, the sample may be treated to extract the nucleic acids contained therein. It will be understood that the particular method used to extract DNA will depend on the nature of the biological sample.
  • the resulting nucleic acid from the sample may be subjected to gel electrophoresis or other size separation techniques, or, the nucleic acid sample may be immobilized on an appropriate solid matrix without size separation.
  • diagnostic assays may be used to monitor PSA-3 agonist polynucleotide levels during therapeutic treatment or intervention.
  • PSA-3 agonist polynucleotide sequences, or fragments, or complementary sequences thereof can be used in Southern or Northern analysis, dot blot, or other membrane-based technologies; in PCR technologies; or in dip stick, pin, ELISA or biochip assays utilizing fluids or tissues from patient biopsies to detect the status of, e.g., levels of PSA-3 agonist expression.
  • Such qualitative or quantitative methods are well known in the art (G.H. Keller and M.M. Manak, 1993, DNA Probes, 2 nd Ed, Macmillan Publishers Ltd., England; D.W. Dieffenbach and G. S. Dveksler, 1995, PCR Primer. A Laboratory Manual, Cold Attorney Docket No.: 38163-0166
  • Methods suitable for quantifying the expression of PSA-3 agonist nucleic acids include radiolabeling or biotinylating nucleotides, coamplification of a control nucleic acid, and standard curves onto which the experimental results are interpolated (P.C. Melby et al., 1993, J. Immunol Methods 159:235-244; and C. Duplaa et al, 1993, Anal. Biochem. 212(l):229-36.).
  • the speed of quantifying multiple samples may be accelerated by running the assay in an ELISA format where the oligomer of interest is presented in various dilutions and a spectrophotometric or colorimetric response gives rapid quantification.
  • microarray fonnats i.e., DNA chips or biochips
  • D.A. Rew DA 2001, Eur. J. Surg. Oncol. 27(5):5048; P.J. Planet et al., 2001, Genome Res. 11(7):1149-55; J. Quackenbush, 2001, Nat. Rev. Genet. 2(6):418-27; O.P. Kallioniemi et al., 2001, Hum. Mol . Genet. 10(7):657- 62; U.S. Patent No. 6,015,702 to P. Lai et al; M. Schena (Ed.), 2000, Microarray Biochip Technology, Eaton Publishing).
  • Kits suitable for nucleic acid-based diagnostic applications typically include the following components:
  • Probe DNA The probe DNA may be prelabeled. Alternatively, the probe DNA may be unlabeled and the ingredients for labeling may be included in the kit in separate containers. Probes may hybridize to PSA-3 agonist nucleic acids, or longer PSA nucleic acids comprising PSA-3 agonist nucleic acids; and
  • Hybridization reagents The kit may also contain other suitably packaged reagents and materials needed for the particular hybridization protocol, including solid- phase matrices, if applicable, and standards.
  • one or more PSA-3 agonist peptides are administered to a host via a vector (e.g., plasmid or viral vector).
  • a vector e.g., plasmid or viral vector.
  • the preferred host is human.
  • a specific immune response for PSA can be generated by administering between about 105 -109 pfu of the recombinant pox virus, constructed as discussed above to a host, more preferably Attorney Docket No.: 38163-0166
  • 10' pfu can be administered. At least one interval thereafter, which is preferably one to three months later, the immune response is boosted by administering additional antigen to the host. More preferably there is at least a second "boost" preferably one to three months after the first boost.
  • one or more cytokines e.g., IL-2, IL-6, IL-12, RANTES,
  • GM-CSF, TNF- , or IFN-y growth factors, e.g., GM-CSF or G-CSF; or costimulatory molecules, e.g., ICAM-1, LFA-3, CD72, B7-1, B7-2, or other B7related molecules; or OX-40L or 41 BBL; or combinations thereof; may be used as biological adjuvants (see, e.g., MX. Salgaller et al., 1998, J. Surg. Oncol. 68(2):122-38; M.T. Lotze et al, 2000, Cancer J. Sci. Am. 6(Suppl l):S61-6; L.
  • genes encoding the molecules can be administered systemically to the host, or co-administered via insertion of the genes encoding the molecules into a vector, for example, a recombinant pox vector (see, e.g., U.S. Patent No. 6,045,802 to Schlom et al.).
  • these genes' may be cloned into same vector as the PSA-3 agonist coding sequence, or the genes may cloned into one or more separate vectors for co-administration.
  • nonspecific immunomodulating factors such as Bacillus Calmette-Guerin (BCG) and levamisole can be co-administered.
  • an adjuvant may be preferable to administer an adjuvant to further increase the immune response in the subject.
  • adjuvants are known and used by those skilled in the art. Examples of adjuvants suitable for human use include, but are not limited to, alum, aluminum salts, aluminum phosphate, aluminum hydroxide, aluminum silica, Montanide (e.g., ISA 50, ISA 51, ISA 80, ISA 206, ISA 720, ISA 740), and calcium phoshate (e.g., nanoparticles; BioSante Phannaceuticals, Inc., Lincolnshire, IL).
  • a preferred adjuvant is RTBI adjuvant (e.g., Detox®, Corixa Corp., Seattle WA).
  • Detox® includes three components extracted from bacteria, monophosphoryl lipid A, trehalose dimycolate and cell wall skeleton (TDM+CWS+MPL®; Corixa Corp.) in a 2% squalene/Tween 80 emulsion.
  • Other preferred adjuvants include BCG, ISCOM® and ISCOMATRIX® (CSL Limited, Parkville, Australia) and aluminum hydroxide adjuvant (Superphos, Biosector).
  • the recombinant vector can be administered using any acceptable route, including, for example, scarification and injection, e.g., intradermal, subcutaneous, intramuscular, Attorney Docket No.: 38163-0166
  • the recombinant vectors will typically be injected in a sterile aqueous or non-aqueous solution, suspension or emulsion in association with a phannaceutically-acceptable carrier such as physiological saline.
  • a host cell e.g., CTLs
  • the PSA-3 agonist peptide or compositions of the invention can be co-administered with an antigen presenting cell, such as a dendritic cell or a B-cell.
  • Cytotoxic T cells specific for an PSA- 3 agonist peptide can be established from peripheral blood mononuclear cells (PBMC) obtained from a host immunized as discussed above.
  • PBMC peripheral blood mononuclear cells
  • the cytotoxic T cell can be cultured to amplify its number and then injected back into the host by a variety of means.
  • cytotoxic T cells per 5 infusion are administered in, for example, one to three infusions of 200 to 250 ml each over a period of 30 to 60 minutes.
  • the patient may be treated with recombinant interleukin-2 with a dose of 720,000 IU per kilogram of body weight intravenously every eight hours; some doses can be omitted depending on the patient's tolerance for the drug.
  • additional antigen or fragments containing T cell eliciting epitope(s) may be administered to the patient to further expand the T cell number.
  • the antigen or epitope may be formulated with an adjuvant and/or may be in a liposomal formulation.
  • the cytotoxic T cells can also be modified by introduction of a viral vector containing DNA encoding one or more PSA-3 agonist peptides, polypeptide comprising these peptides, and/or TNF-a . These modified cells can be reintroduced into a host in an effort to enhance the anti-tumor activity of the cells.
  • Other cytokines or modulators can also be used, as described in detail herein.
  • compositions comprising one or more PSA-3 agonist peptides (e.g., SEQ ID NO:3-SEQ ID NO:5), or PSA polypeptides comprising these peptides (e.g., SEQ ID NO:25-SEQ ID NO:30), or fragments or variants thereof, and a physiologically acceptable carrier, excipient, or diluent.
  • PSA-3 agonist peptides e.g., SEQ ID NO:3-SEQ ID NO:5
  • PSA polypeptides comprising these peptides (e.g., SEQ ID NO:25-SEQ ID NO:30), or fragments or variants thereof, and a physiologically acceptable carrier, excipient, or diluent.
  • a pharmaceutical composition includes, in admixture, a Attorney Docket No.: 38163-0166
  • compositions comprising these peptides, or fragments or variants, as described herein, as active ingredients.
  • compositions that contain polypeptides or peptides as active ingredients are well understood in the art.
  • such compositions are prepared as injectables, either as liquid solutions or suspensions, however, solid forms suitable for solution in, or suspension in, liquid prior to injection can also be prepared.
  • the preparation can also be emulsified.
  • the active therapeutic ingredient is often mixed with excipients that are pharmaceutically acceptable and compatible with the active ingredient. Suitable excipients are, for example, water, saline, dextrose, glycerol, ethanol, or the like and combinations thereof.
  • the composition can contain minor amounts of auxiliary substances such as wetting or emulsifying agents, pH-buffering agents, which enhance the effectiveness of the active ingredient.
  • PSA-3 agonist peptides, or PSA polypeptides comprising these peptides can be formulated into the pharmaceutical composition as neutralized physiologically acceptable salt forms.
  • Suitable salts include the acid addition salts (i.e., formed with the free amino groups of the polypeptide or antibody molecule) and which are formed with inorganic acids such as, for example, hydrochloric or phosphoric acids, or such organic acids as acetic, oxalic, tartaric, mandelic, and the like.
  • Salts formed from the free carboxyl groups can also be derived from inorganic bases such as, for example, sodium, potassium, ammonium, calcium, or ferric hydroxides, and such organic bases as isopropylamine, trimethylamine, 2-ethylamino ethanol, histidine, procaine, and the like.
  • inorganic bases such as, for example, sodium, potassium, ammonium, calcium, or ferric hydroxides, and such organic bases as isopropylamine, trimethylamine, 2-ethylamino ethanol, histidine, procaine, and the like.
  • compositions may be produced as neutral or salt forms. Salts can be formed with many acids, including, but not limited to, hydrochloric, sulfuric, acetic, lactic, tartaric, malic and succinic acids. Compositions can take the fonn of solutions, suspensions, suppositories, tablets, pills, capsules, sustained release compounds, or powders. Such formulations can contain 10%-95% (w/w) of the active ingredient, preferably 25%-70% (w/w).
  • compositions can also contain one or more physiologically acceptable carrier(s), excipient(s), diluent(s), disintegrant(s), lubricant(s), plasticizer(s), filler(s), colorant(s), dosage vehicle(s), absorption enhancer(s), stabilizer(s), or bacteriocide(s).
  • physiologically acceptable carrier(s) excipient(s), diluent(s), disintegrant(s), lubricant(s), plasticizer(s), filler(s), colorant(s), dosage vehicle(s), absorption enhancer(s), stabilizer(s), or bacteriocide(s).
  • compositions and preparations are carried out by methods known and practiced in the art.
  • phannaceutical compositions Following the preparation of phannaceutical compositions, they may be placed in appropriate containers and labeled for the treatment of indicated conditions. Such labeling can include amount, frequency, and method of administration. Preparations may be administered systemically by oral or parenteral routes.
  • parenteral routes of administration include subcutaneous, intramuscular, intraperitoneal, intravenous, transdermal, inhalation, intranasal, intra-arterial, intrathecal, enteral, sublingual, or rectal.
  • Intravenous administration for example, can be performed by injection of a unit dose.
  • unit dose when used in reference to a pharmaceutical composition of this invention refers to physically discrete units suitable as unitary dosage for humans, each unit containing a predetermined quantity of active material calculated to produce the desired therapeutic effect in association with the required diluent; i.e., carrier, or vehicle.
  • compositions are administered in a manner compatible with the dosage formulation, and in a therapeutically effective amount.
  • the quantity to be administered depends on the subject to be treated, capacity of the subject's immune system to utilize the active ingredient, and degree of immunostimulation desired. Precise amounts of active ingredient required to be administered depend on the judgment of the practitioner and are specific for each individual. However, suitable dosages may range from about 0.1 mg to 20 mg, preferably about 0.5 mg to about 10 mg, and more preferably one milligrams to several milligrams of active ingredient per kilogram body weight of individual per day, depending on the route of administration. Suitable regimes for initial administration and booster shots are also variable, but are typified by an initial administration followed by repeated doses at one or more hour intervals by a subsequent injection or other administration. Alternatively, continuous intravenous infusions sufficient to maintain concentrations of 10 nM to 10 ⁇ M in the blood are contemplated.
  • An exemplary pharmaceutical formulation comprises: PSA-3 agonist peptide (5.0 mg/ml); sodium bisulfite USP (3.2 mg/ml); disodium edetate USP (0.1 mg/ml); and water for injection q.s.a.d. (1.0 ml). Further guidance in preparing pharmaceutical formulations can be found in, e.g., Gilman et al. (eds), 1990, Goodman and Gilman's: The Pharmacological Basis of Ther-apeutics, 8th ed., Pergamon Press; and Remington's Attorney Docket No.: 38163-0166
  • adjuvants suitable for human use include, but are not limited to, alum, aluminum salts, aluminum phosphate, aluminum hydroxide, aluminum silica, Montanide ISA 720, and calcium phoshate (e.g., nanoparticles; BioSante Pharmaceuticals, Inc., Lincolnshire, IL).
  • a prefened adjuvant is RIBI adjuvant (e.g., Detox®, Corixa Corp., Seattle WA) which contains three components extracted from bacteria, monophosphoryl lipid A, trehalose dimycolate and cell wall skeleton (TDM+CWS+MPL®; Corixa Corp.) in a 2% squalene/Tween 80 emulsion.
  • RIBI adjuvant e.g., Detox®, Corixa Corp., Seattle WA
  • TDM+CWS+MPL® trehalose dimycolate and cell wall skeleton
  • Other prefened adjuvants include BCG, ISCOM® and ISCO
  • one or more cytokines e.g., IL-2, IL-6, IL-12, RANTES, GM-CSF, TNF- ⁇ , or IFN- ⁇ , growth factors, e.g., GM-CSF or G-CSF; or co-stimulatory molecules, e.g., ICAM-1, LFA-3, CD72, B7-1, 1372, or other B7-related molecules; or OX-40L or 41 BBL; or a combination thereof; may be used as biological adjuvants (see, e.g., M.L. Salgaller et al., 1998, J. Surg. Oncol. 68(2): 122-38; M.T.
  • a therapeutically effective amount of a pharmaceutical composition containing one or more PSA-3 peptides, or polypeptides comprising these peptides is an amount sufficient to reduce, ameliorate, or eliminate prostate cancer.
  • An effective amount can be introduced in one administration or over repeated administrations to an individual being treated. Therapeutic administration can be followed by prophylactic administration, after treatment of the disease.
  • a prophylactically effective amount is an amount effective to Attorney Docket No.: 38163-0166
  • the therapeutically effective dose may be estimated initially, for example, either in cell culture assays or in animal models, usually mice, rats, rabbits, dogs, sheep, goats, pigs, or non-human primates.
  • the animal model may also be used to determine the maximum tolerated dose and appropriate route of administration. Such information can then be used to determine useful doses and routes for administration in humans.
  • the peptide-based, vector-based, and cell-based therapies of the invention can be used individually or in any combination.
  • these treatments can be used as adjuncts to other treatments for prostate cancer, including, but not limited to, hormone therapy, chemotherapy, surgery (e.g., radical prostatectomy), cryosurgery, radiation therapy (e.g., external beam or seed implant), interstitial brachytherapy, and immunotherapy (e.g., anti-HER2 antibodies; Herceptin®).
  • hormone therapy e.g., chemotherapy, surgery (e.g., radical prostatectomy), cryosurgery, radiation therapy (e.g., external beam or seed implant), interstitial brachytherapy, and immunotherapy (e.g., anti-HER2 antibodies; Herceptin®).
  • the human prostate carcinoma cell line LNCaP (M.G.
  • HLA-A2 positive and PSA negative human melanoma cell line
  • VA American Type Culture Collection
  • the cultures were free of mycoplasma and were maintained in complete medium (RPMI 1640; Life Technologies,
  • the C1R cell line is a human plasma leukemia cell line that does not express endogenous HLA-A or B antigens (K.S. Anderson et al., 1993, J. Immunol. 151:3407- 3419).
  • C1R-A2 cells are Cl R cells that express a transfected genomic clone of HLA- A2.1 (W.J. Storkus et al., 1987, J. Immunol, 138:16571659). These cells were obtained from Dr. William E. Biddison (National Institute of Neurological Disorders and Stroke, NTH, Bethesda, MD).
  • the 174CEM-T2 cell line (T2) transport deletion mutant (K.T. Attorney Docket No.: 38163-0166
  • V8T cell line a cytotoxic T lymphocyte (CTL) line directed against the carcinoembryonic antigen (CEA) CAP-1 epitope
  • CTL cytotoxic T lymphocyte
  • CEA carcinoembryonic antigen
  • V8T cells were restimulated with CAP-1 peptide (25 ⁇ g/ml) on day 16 after prior restimulation at an effector to APC ratio of 1:3. Irradiated (23,000 rads) autologous EBV transformed B cells were used as APCs.
  • EXAMPLE 2 Peptides A panel of analogs with single or double amino acid substitutions at positions PI, P2 and P10 of PSA peptide PSA-3 (P. Coneale et al., 1997, J. Nat. Cancer Inst. 19:293-300) ( Figure 1), and a CEA peptide CAP1-6D (S. Zaremba et al., 1997, Cancer Res. 57:45704577), were greater than 96% pure.
  • the cells were washed three times and incubated with a 1:100 dilution of fluorescein isothiocyanate (FITC)-labeled goat anti-mouse immunoglobulin (IgG) (Kirkegaard and Peny Laboratories, Gaithersburg, MD).
  • FITC fluorescein isothiocyanate
  • IgG goat anti-mouse immunoglobulin
  • the cells were immediately analyzed using a Becton Dickinson FACScan equipped with a blue laser with an excitation of 15 nW at 488 nm. Data were gathered from 10,000 live cells, stored and used to generate results.
  • Dual-color flow cytometric analysis The procedure for dual-color flow cytometric analysis was similar to that for single-color analysis with the following exceptions.
  • the antibodies used were anti-CD4 FITC/anti-CD8 PE, anti-CD45R0- FITC/anti-CD49d PE, anti-CD28 FITC/anti-CD56 PE, anti-CD86 FITC/anti-CD80 PE, anti-CD58 FITC/anti-CD54 PE, anti-MHC class I FITC/anti-MHC class II PE, and anti- IgGl FITC/anti-IgG2a PE (isotype controls).
  • Antibodies to CD4, CD8, CD28, CD45R0, CD56, CD49d, CD 54, CD80, CD86, and CD58 were purchased from Becton Dickinson.
  • Antibodies to MHC-class I and MHC-class II were purchased from Serotec, UK.
  • Antibodies to CD 14 and CD54 were purchased from Becton Dickinson. Staining was done simultaneously for 1 h, after which cells were washed three times, resuspended as above, and immediately analyzed using a Becton Dickinson FACScan equipped with a blue laser with an excitation of 15 nW at 488 nm with the use of the CELLQuest program (Becton Dickinson, San Jose, CA).
  • HLA-A2 normal donor PBMCs peripheral blood mononuclear cells
  • PBMCs peripheral blood mononuclear cells
  • lymphocyte separation medium gradient Organon Teknika, Durham, NC
  • DCs Dendritic cells
  • PBMCs (1.5 x 10 8 ) were resuspended in AIM-V medium containing 2 mM glutamine, 50 Ng/ml streptomycin, and 10 ⁇ g/ml gentamycin (Life Technologies, hie), and allowed to adhere to a T-150 flask (Corning Costar Corp., Cambridge, MA).
  • the non-adherent cells were removed with a gentle rinse.
  • the adherent cells were cultured for 6-7 days in AIM-V medium containing 100 ng/ml of recombinant human GM-CSF (rhGM-CSF) and 20 ng/ml of recombinant human IL-4 (rhIL-4) and 20 ng/ml of TNF- ⁇
  • the culture medium was replenished every 3 days.
  • PSA cDNA was inserted under the control of the vaccinia 40K promoter (L. Gritz et al, 1990, j. Virol. 64:5948-5957) into the Hindlll M genomic region of the Wyeth strain of vaccinia virus.
  • the E. coli lacZ gene under the control of the fowlpox Cl promoter (S. Jenkins et al., 1991, AIDS Res. Hum. Retroviruses 7:991-998), was included as a colorimetric marker for recombinant viruses.
  • Recombinant virus was identified using a chromogenic assay for the lacZ gene product, as described previously (D. Panicali et al., 1986, Gene 47:193-199).
  • codon 155 in the PSA sequence was changed from ATT (isoleucine) to CTG (leucine) by in vitro mutagenesis (G. Mazzara et al., 1993, Methods Enzymol. 217: 557-581, K. Smith et al., 1993, Vaccine 11:43-53).
  • PSA-3A The resulting PSA sequence, designated PSA-3A, was inserted under the control of the vaccinia 40K promoter into the Hindlll M genomic region of a derivative of the Wyeth strain of vaccinia virus using a hostrange selection system, as described previously (G. Mazzara et al., 1993, Meth. Enzymol. 217:557-581; K. Smith et al., 1993, Vaccine 11:43- 53, 1993).
  • DCs (1 x 10 6 ) were incubated in 1 ml of Opti-MEM medium (Life Technologies, Inc.) at 37°C with rV-PSA, rV-PSA-3A or control vaccinia virus vector.
  • T cell Lines Modification of the protocol described by Tsang et al. (K.Y. Tsang et al, 1997, Clin. Cancer Res. 3:2439-2449) was used to generate PSA- specific CTL.
  • DCs were used as APCs and nonadherent cells isolated from PBMCs were used as a source of effector cells.
  • PSA-3 or PSA-3A peptide was added to the DCs at a final concentration of 25 ⁇ g/ml.
  • Autologous non-adherent cells were then added to APCs at an APC to effector ratio of 1:10. Cultures were incubated for 3 days at 37° C in a humidified atmosphere containing 5%> C0 2 .
  • the cultures were then supplemented with recombinant human IL-2 at a concentration of 20 units/ml for 7 days.
  • the IL-2 containing medium was replenished every 3 days.
  • the 3-day incubation with peptide and 7-day IL-2 supplement constituted one in vitro stimulation (TVS) cycle.
  • Primary cultures were restimulated with PSA peptide (25 ⁇ g/ml) on day 11 to begin the next IVS cycle.
  • Irradiated autologous DCs were used as APC for three IVS cycles.
  • Lrradiated (23,000 rads) autologous EBV-transformed B cells were used as APC after the third IVS cycle.
  • Target cells (Cl R-A2 or tumor cells) were labeled with 50 ⁇ Ci of ⁇ h ⁇ dium-labeled oxyquinoline (Medi-Physics Inc., Arlington, IL) for 15 min at room temperature.
  • Target cells (0.3 x 10 4 ) in 100 ⁇ l of RPMI-1640 complete medium were added to each of 96 wells in flatbottomed assay plates (Corning Costar Corp.).
  • Labeled Cl R-A2 target cells were incubated with peptides at the concentration indicated for 60 min at 37°C in 5% CO 2 before adding effector cells. No peptide was used when carcinoma cell lines were used as targets.
  • Effector cells were suspended in 100 ⁇ l of RPMI-1640 complete medium supplemented with 10% pooled human AB serum and added to the target cells. The cells were then incubated at 37° C in 5% C0 2 for 4 or 16 h. Supernatant was harvested for gamma counting with the use of harvester frames (Skatron, Inc., Sterling, VA). Determinations were carried out in triplicate, and standard deviations were calculated. Specific lysis was calculated with the use of the following formula (all values in cpm): Attorney Docket No.: 38163-0166
  • T cells were incubated for 48 h in the presence of peptide-pulsed autologous B cells as described in the IVS procedure, above, and replated to 96-well plates for 24 h. Apoptosis was analyzed using the terminal deoxynucleotidyl transferase- mediated nick-end labeling (TUNEL) assay (Y. Gavrieli et al., 1992, J. Cell Biol. 119:493-
  • HLA-A2.1/K transgenic mice were kindly provided by Dr. L.
  • mice express the product of the HLA-A2.1/Kb chimeric gene in which the alpha-3 domain of the heavy chain is replaced by mouse H-2/K b domain, but the HLA-A2.1 alpha-1 and alpha-2 domains are unaltered (A. Vitiello et al., 1991, J. Exp. Med. 173:1007-1015; V.H. Engelhard et al., 1991, J. Immunol. 46:1226-1232).
  • HLA-A2.1/Kb chimeric gene in which the alpha-3 domain of the heavy chain is replaced by mouse H-2/K b domain, but the HLA-A2.1 alpha-1 and alpha-2 domains are unaltered (A. Vitiello et al., 1991, J. Exp. Med. 173:1007-1015; V.H. Engelhard et al., 1991, J. Immunol. 46:1226-1232).
  • HLA- A2.1/K transgenic mice Three groups of HLA- A2.1/K transgenic mice (three mice per group) were immunized s.c. (subcutaneously) in the base of the tail with PSA-3 peptide-pulsed HLA-A2.1/K b DC, PSA-3 A peptide-pulsed DCs from HLA-A2.1/K b transgenic mice, or DCs only. Peptides were used at a concentration of 50 ⁇ g/ml and DCs were used at 1 x 10 6 cell/mouse/injection. A total of three injections were given to each animal, 2 weeks apart. Mice injected with DCs only were used as controls.
  • mice were sacrificed 7 days after the last injection, and spleen cells were restimulated in vitro with 25 ⁇ g/ml of PSA-3 or PSA3A peptide with inadiated syngeneic spleen cell for 6 days. The cytokine production of these bulk cultures was tested. Peptide-pulsed Jurkat A2 (JA2K b ) cells were used as stimulator cells. Jurkat 0201 Attorney Docket No. : 38163 -0166
  • K b cells are stable transfectants of the human T cell leukemia line, Jurkat, which express the product of HLA-A0201K chimeric gene (L.A. Sherman et al, 1992, Science 258:815- 818).
  • EXAMPLE 12 Detection of Cytokines.
  • Cytometric Bead Anay (CBA) system (BD PharMingen, San Diego, CA) was also used to determine the secretion of multiple cytokines by specific T cell lines.
  • the CBA system uses the fluorescence detection by flow cytometry to measure soluble analytes in a particle-based immunoassay.
  • the BD human Thl/Th2 cytokine CBA Kit was employed to measure IL-2, IL-4, IL-5, IL-10, TNF- ⁇ ; and IFN- ⁇ protein levels in a single sample.
  • the cytokine capture beads were mixed with PE-conjugated detection antibodies and then incubated with recombinant cytokine standards or test samples to form sandwich complexes.
  • the samples results were generated in graphical and tabular format using BD
  • PSA analogs Parental nonamer PSA-3 peptide (amino acid position 154-163 of PSA) and analog nonamers. Amino acids are shown by the single-letter code. Substitution amino acids are indicated in bold font.
  • conesponding nucleotide sequences are shown in the table, below. Substitution codons are indicated in bold font.
  • Figure 2 shows that PSA-3A-HLA-A2 complexes were more stable than PSA-3 complexes over the 8-h observation period.
  • both the ability of the peptide to bind MHC ( Figures 1A-1 B) and the stability ( Figure 2), i.e., avidity of the peptide-MHC complex are greater for the PSA-3A peptide than the native PSA-3 peptide.
  • T-PSA-3A The line established with peptide PSA-3A, designated T-PSA-3A, was shown to lyse C1R-A2 cells pulsed with peptide PSA-3A to a greater extent than cells pulsed with the PSA-3 peptide ( Figure 3A). T cells established using the PSA-3 peptide, however, also lysed target cells pulsed with the PSA-3A peptide to a greater extent than those pulsed with the PSA-3A peptide ( Figure 3B). This was seen at two different effector to target cell ratios. To further analyze this phenomenon, Cl R-A2 cells were then pulsed with different concentrations of the native and agonist peptides and used as targets for the two T cell lines.
  • T cells generated with the PSA-3A peptide showed a greater percent lysis of target cells pulsed with the PSA-3A peptide than cells pulsed with the PSA-3 peptide at each peptide concentration; approximately 8-fold less PSA-3 A peptide than PSA-3 peptide was necessary for lysis ( Figure 4A). Moreover, this phenomenon was also observed using T cells established with the native PSA-3 peptide. Thus, these T cells lysed C1R-A2 target Attorney Docket No.: 38163-0166
  • T-PSA-3 The T cell lines established with peptide PSA-3 (designated T-PSA-3) and peptide PSA-3A (designated T-PSA-3A) were both shown to be > 95% positive for CD49d, > 67% positive for CD8 + , ⁇ 3.0% positive for CD56 + , and > 88% positive for CD45R0 + cells.
  • T cells stimulated with autologous B cells pulsed with either peptide were analyzed at IVS-5 for DNA fragmentation by the TUNEL assay.
  • Figure 5 shows that 2.9% apoptotic CD8 + cells were observed in the absence of peptide (Figure 5A), 4.9% apoptotic CD8 + cells were observed in cells stimulated with PSA-3 peptide ( Figure 5B), and 4.5% apoptotic CD8 + cells were observed when cells were stimulated with PSA-3 peptide ( Figure 5C). Thus, no difference in apoptosis was seen in CD8 T cells stimulated with the agonist peptide as compared to the native peptide.
  • cytokine profile of T cells stimulated with APCs pulsed with either the PSA-3 or the PSA-3 A peptide was then analyzed.
  • the T cell line derived using the PSA-3 peptide was used in these studies, and the APCs used were autologous B cells.
  • a Cytometric Bead Array (CBA) assay was used for analysis (see Examples section) using supernatant fluids obtained 24 h after stimulation.
  • Figures 6A-6C illustrate four of the 10 internal standards used for the calibration of the results obtained in this assay.
  • Figures 6D-6F show the levels of each of six cytokines produced by T cells stimulated with APCs pulsed with no peptide, PSA-3A peptide, and PSA-3 peptide, respectively.
  • T cells were also conducted to determine the level of IFN- ⁇ production by T cells, originally generated with the PSA-3 A peptide, when stimulated with DCs that were pulsed with the PSA-3 and PSA-3A peptides.
  • Table 2 shows that T cells stimulated with Attorney Docket No.: 38163-0166
  • DCs pulsed with the PSA-3 A peptide produce more IFN- ⁇ than those stimulated with DCs pulsed with the PSA-3 peptide.
  • Cultures devoid of peptide, DCs, or T cells demonstrated the specificity of the IFN- ⁇ production (Table 2), and the lack of non-specific anti- allogeneic reactivity.
  • Table 2 Production of IFN- ⁇ by a T cell line stimulated with PSA-3 or agonist PSA-3A peptides.
  • the PSA-specific T cell line T-PSA-3A was used as effector cells at IVS-3.
  • T- PSA-3A cells were stimulated with kradiated HLA-A2 positive allogeneic DCs either pulsed with PSA-3 or PSA-3 A peptide at a concentration of 25 ⁇ g/ml and an effector-to- APC ratio of 10:1.
  • APC antigen producing cell.
  • Table 3 The ability of DCs pulsed with peptides PSA-3 or PSA-3 A agonist to produce IL- 12.
  • the PSA-specific T cell lines T-PSA-3A (derived by pulsing PBMC with the PSA-3A peptide) and T-PSA-3 (derived by pulsing PBMC with the PSA-3 peptide) were used as effector cells at IVS-4.
  • T cells 15 were stimulated with HLA-A2 positive allogeneic DCs either pulsed with PSA-3 or PSA-3A peptide at a concentration of 25 ⁇ g/ml and an effector-to-APC ratio of 10:1.
  • 24-h culture supematants were collected and screened for the secretion of IL-12.
  • IL-12 production is expressed as pg/ml/5 x 10 5 DC.
  • T-PSA-3A line was capable of lysing the LNCaP human prostate carcinoma cell line that expresses native PSA and was HLA-A2 positive.
  • the HLA-A2 positive SK-mel human melanoma line that does not express PSA showed no lysis.
  • the T- PSA-3 line (generated with the native PSA-3A peptide) also lysed the LNCaP line, but at lower levels than that observed with the T-PSA-3 A line at each effector to target cell ratio (Table 4).
  • Table 4 shows that the lysis of the LNCaP tine by the T- PSA-3A line was blocked by the anti-HLA-A2 antibody and not by the isotype matched control antibody UPC- 10.
  • Table 4 Ability of T cells generated with agonist peptide (PSA-3 A) to lyse prostate cancer cells expressing native PSA.
  • PSA-3 A agonist peptide
  • LNCaP human prostate carcinoma
  • SK-mel melanoma
  • Experiments 1 and 2 were conducted at IVS 3 and 4, respectively. E:T ratio for experiment 2 was 25:1. The number in parentheses is the standard deviation.
  • LNCaP cells (1 x 10 6 ) were labeled with '"h and incubated for 1 h in the presence of medium containing no antibody, control antibody UPC-10 (10 ⁇ g/ml), or anti-HLAA2,28 antibody (1:100 dilution). Cells were used as targets in an 18-h cytotoxic assay. * Statistical significant (PO.01, two-tailed t test).
  • the HLA-A2/K transgenic mouse has been previously reported to aid in the determination of the immunogenicity of HLA-A2 peptides for humans. This in vivo system was thus employed to further analyze and compare the immunogenicity of the PSA-3A peptide with that of the native PSA-3 peptide.
  • DCs from the HLA-A2/K transgenic mice were pulsed with either the PSA-3 or the PSA-3A peptide and used to vaccinate HLA-A2/K mice. DCs alone (no peptide) were also used as a control vaccine. After three vaccinations at 2-week intervals, T cells were isolated from splenocytes obtained 2 weeks after the last vaccination.
  • T cells were then incubated with Jurkat A2/K b cells pulsed with the PSA-3 peptide, the PSA-3A peptide, or no peptide, and production of INF- ⁇ was measured from supematants after 24 h.
  • Table 5 shows that the use of DCs alone with no peptide as immunogen resulted in no TNF- ⁇ production by T cells, hi contrast, T cells obtained from mice vaccinated with DCs pulsed with the PSA-3 peptide did produce LNF- ⁇ when APCs were pulsed with either peptide PSA-3 or PSA3A (Table 5). However, much higher levels of INF- ⁇ , were produced from T cells of mice vaccinated with DCs pulsed with the PS A-3 A peptide when stimulated with Jurkat A2/K cells pulsed with either the native or agonist PSA peptide (Table 5). These studies thereby provide additional evidence that the PSA- 3 A epitope is more immunogenic than the PSA-3 epitope in the context of the HLA-A2 allele.
  • T cells were obtained from mice immunized with DCs only, PSA-3 pulsed DCs, or PSA-3A pulsed DCs. Three mice were used in each group. Three injections (1 x 10 6 DC/mouse/injection) were given to each animal at 2-week intervals. Peptides were used at a concentration of 50 ⁇ g/ml. T cells obtained from HLA-A2/K transgenic mice were stimulated with PSA-3 or PSA-3A peptide (25 ⁇ g/ml) pulsed Jurkat A2/K b cells in the IFN- ⁇ production assay. Twenty-four h culture supematants were collected and screened for the secretion of IFN- ⁇ .
  • Recombinant vaccinia viruses were thus constructed with the entire PSA transgene without and with the amino acid change of isoleucine to leucine at position 155. These recombinant vaccinia viruses were designated rV-PSA and rV-PSA-3A, respectively.
  • Initial studies showed the optimal multiplicity of infection for human DCs for both recombinant vaccinia viruses to be 10 pfu per cell. Human DCs infected with either of the recombinant vectors showed the production of PSA protein at approximately 63 ng/ml as determined by immunoassay of supernatant fluids.
  • DCs infected with either rV-PSA or rV-PSA-3A were used to stimulate T cells originally derived by pulsing APC with the native PSA-3 peptide.
  • noninfected DCs pulsed with 25 ⁇ g of the PS A-3 A peptide were also used to activate T-PSA-3 T cells.
  • no activation of the CEA-specific T cell line (V8T) was observed by the PSA recombinant vectors.
  • DCs infected with wild-type vaccinia vector were used.
  • Table 6 Ability of DCs infected with vaccinia PSA recombinants to process the PS A-3 A agonist epitope to activate PSA-specific T cells.
  • PSA-specific T-PSA-3 cells and CEA- specific V8T cells were stimulated with inadiated allogeneic DCs either uninfected or infected with rV-PSA, rV-PSA (PSA-3A), or V-WT (wild type).
  • uninfected DCs or DCs infected with V-WT were pulsed with PSA-3A peptide or the CAP1-6D peptide.
  • Peptides were used at a concentration of 25 ⁇ g/ml.
  • Vaccinia vims vector infections were at a MOI of 10 for 1-h. Infected cells were then incubated overnight in completed medium at 37° C and used as APC. Forty-eight h culture supematants were collected and screened for the secretion of IFN- ⁇ ,
  • the CAP1-6D peptide is a TCR-agonist of the CEA peptide CAP-1.
  • the results presented here demonstrate that the agonist peptide PSA-3A epitope is superior to the native PSA-3 epitope in terms of affinity of binding to MHC, avidity of the peptide MHC complex, and ability to activate CTL in vitro.
  • the agonist epitope was also more efficient than the native epitope in T cell activation in an in vivo HLA-A2.11K b transgenic mice model (P. Coneale et al., 1998, J. Immunol. 161:3186-3194).
  • T cells activated by the PSA-3A peptide had the ability to lyse both APCs pulsed with native peptide and human prostate cancer cells expressing native PSA in an MHCrestricted manner.
  • PSA-3 peptide to the HLA-A2.1 molecule This may be explained partially by the fact that L at position 9, instead of V, reduced the peptide-HLA- A2.1 affinity as well as the complexes' stability (j. Ruppert et al., 1993, Cell 74:929-937; D. R. Madden, 1995, Ann. Rev. Immunol 13:387-622). It has been demonstrated that in the case of Flu A matrix HLA-A2.1 binding 58-66 (GILGFVFTL; SEQ ID NO:6) and 58-68 (GILGFVTLVL; SEQ ID NO:7), no decrease in binding to HLA-A2 was detected when V, instead of L, was at the C-terminal (H.W.
  • Residues strongly associated with poor HLA-A2.1 binding at the secondary anchor position are D, E, P at position 1; D, E at position 3; R, K, H, A at Attorney Docket No.: 38163-0166
  • a gplOO peptide 280-288 contains the predicted motif residues Y at position 1, L at position 2, and A at position 9. These residues are predicted to support good binding to the HLA-A2.1 molecule, but the actual binding affinity of this peptide was not high. The lower affinity of the peptide may be due to residues at other positions of the peptide, such as a negatively charged E at position 3 (Y. Kawakami et al., 1995, J. Immunol. 154:3961-3968; A.L. Cox et al, 1994, Science 264:716-719).
  • a melanoma gplOO peptide with an altered anchor residue used in combination with IL-2 produced more clinical responses in melanoma patients than a native gplOO peptide used in combination with IL-2 (S.A. Rosenberg et al., 1999, J. Immunol. 163:1690-1695).
  • one of the amino acids of the CEA peptide CAPl that interacts with the T cell receptor (TCR) was modified to generate the CAP1-6D TCR enhancer agonist epitope (S. Zaremba et al., 1997, Cancer Res. 57:4570-4577).
  • DCs pulsed with the CAP1-6D agonist were used as a vaccine in patients with advanced CEAexpressing carcinomas (L. H. Fong et al., Amer. Assoc. for Cancer Res. Ann. Mtg. April 1-5, 2000 Proceedings #1387, 41:217).
  • serum CEA stabilization was seen in a subset of patients and regression of lung metastases was observed.
  • CEA-specific T cell responses were also generated in patients using the agonist epitope (L.H. Fong et al., Amer. Assoc. for Cancer Res. Ann. Mtg. April 1-5, 2000 Proceedings #1387, 41:217).
  • the agonist PSA-3A peptide described herein is useful either as a peptide vaccine in adjuvant or via peptide-pulsed DCs in vaccine therapy for prostate cancer patients positive for the HLA-A2 allele.
  • Flt-3L E. Maraskovsky et al, 1996, J. Exp. Med. 184:1953-1962; S.D. Lyman, 1995, Int. J. Hematol 62:63-73
  • TRICOM vectors i.e., vectors containing three costimulatory molecules (J.W. Hodge et al., 2000, J. Natl. Cancer Inst. 92:1228-1239), allow researchers to successfully pursue DC vaccine protocols.
  • Increases in the production of IL-5 by the activated T cells may in turn activate eosinophils, basophils, B cells, and thymocytes.
  • IL-5 is a chemotactic and activating factor for eosinophils.
  • IX-5 has also been shown to exhibit a killer-helper factor activity on peanut agglutinin binding thymocytes in the presence of stimulator cells and IL-2. This results in the recraitment of CTL from among the thymocyte population due to the ability of IL-5 to upregulate IL-2 receptors on target thymocytes (K. Takatsu et al., 1987, Proc. Natl. Acad. Sci.
  • PSA-3 A peptide may also be used in more sensitive immunoassays to monitor immune responses of patients involved in PSA vaccine clinical trials.
  • PSA-based vaccines Several clinical trials using PSA-based vaccines have been completed or are in progress in patients with prostate cancer.
  • a recent study in patients with advanced prostate cancer demonstrated that an rVPSA vaccine induced specific T cell responses for the PSA- 3 peptide in five of seven HLA-A2.1 patients vaccinated (J.P. Eder et al, 2000, Clin. Cancer Res. 6:1632-1638).
  • the rV-PSA vaccine was shown to be safe, and certain patients remained without evidence of clinical progression for at least 21 months (J.P. Eder et al., 2000, Clin. Cancer Res. 6:1632-1638). Ongoing clinical trials are employing Attorney Docket No. : 38163-0166
  • rV-PSA as a primary vaccination, followed by multiple booster vaccinations with a recombinant fowlpox-PSA vaccine.
  • This diversified prime and boost vaccine strategy has shown to be advantageous in both animal models (J.W. Hodge et al., 1997, Vaccine 15:759-768, 1997) and clinical trials (J.L. Marshall et al., 2000, J. Clin. Oncol. 18:3964- 3973) using recombinant CEA vector vaccines.
  • PBMC can be separated using Lymphocyte Separation Medium gradient (Organon Teknika, Durham, NC) as previously described (Boyum et al., 1968, Scand. J. Clin. Lab. Invest. 21:77-80). Washed PBMC are resuspended in a complete medium, for example, RPMI 1640 (GIBCO) supplemented with 10% pool human AB semm (Pel-Freeze Clinical System, Brown Dear, Wis.), 2 mM glutamine, 100 U/ml penicillin and 100 ⁇ g/ml of streptomycin (GIBCO).
  • PBMC at a concentration of about 2 x 10 5 cells in complete medium in a volume of, for example, 100 ⁇ l are added into each well of a 96-well flat-bottom assay plate (Costar, Cambridge, Mass., USA).
  • the antigen or peptides are added into the cultures in a final concentration of about 50 ⁇ g/ml and incubated at 37° C in a humidified atmosphere containing 5% CO 2 for 5 days. After removal of peptide containing media, the cultures are provided with fresh human IL-2 (10 U/ml) after 5 days and replenished with IL-2 containing medium every 3 days. Primary cultures are restimulated with the same peptide (50 ⁇ g/ml) on day 16. Following this, 5 x 10 5 inadiated (4,000 rad) autologous PBMC are added in a volume of about 50 ⁇ l complete medium as antigen-presenting cells (APC). About five days later, the Attorney Docket No.: 38163-0166
  • cultures are provided with human IL-2 containing medium as described previously. Cells are restimulated for 5 days at intervals of 16 days.

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Abstract

L'invention porte sur ses peptides isolés consistant en épitopes agonistes de l'antigène spécifique de la prostate (PSA), et, dans certains de ses aspects, sur des peptides consistant en épitopes agonistes de l'épitope du PSA-3 (du lymphocyte T cytotoxique) et en peptides codant pour les acides nucléiques dont les épitopes agonistes du PSA-3. L'invention porte également sur des sondes, amorces, et vecteurs comprenant lesdits acides nucléiques, ainsi que sur des cellules hôtes comprenant ces vecteurs et sur des anticorps de fixant aux peptides agonistes du PSA-3. L'invention porte en outre sur des réactifs de diagnostic, sur des procédés utilisant les acides nucléiques et anticorps de l'invention, sur des préparations pharmaceutiques comportant les acides nucléiques, les cellules hôtes et les peptides de l'invention, sur des procédés de traitement ou prévention du cancer de la prostate utilisant lesdites préparations par exemple pour des immunothérapies médiées par lesdits peptides, cellules et vecteurs.
PCT/US2002/037805 2001-11-30 2002-11-26 Peptides agonistes d'antigenes specifiques de la prostate et leurs utilisations WO2003047506A2 (fr)

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DE60235041T DE60235041D1 (de) 2001-11-30 2002-11-26 Und ihre verwendung
AT02789873T ATE454447T1 (de) 2001-11-30 2002-11-26 Peptidagonisten für prostata-spezifisches antigen und ihre verwendung
CA2468258A CA2468258C (fr) 2001-11-30 2002-11-26 Peptides agonistes d'antigenes specifiques de la prostate et leurs utilisations
AU2002352913A AU2002352913B2 (en) 2001-11-30 2002-11-26 Peptide agonists of prostate-specific antigen, and uses therefor
JP2003548767A JP4364643B2 (ja) 2001-11-30 2002-11-26 前立腺特異抗原のペプチドアゴニストおよびその使用
EP02789873A EP1461073B1 (fr) 2001-11-30 2002-11-26 Peptides agonistes d'antigenes specifiques de la prostate et leurs utilisations
DK02789873.3T DK1461073T3 (da) 2001-11-30 2002-11-26 Peptidagonister til prostataspecifikt antigen og anvendelser heraf
US10/497,003 US7247615B2 (en) 2001-11-30 2002-11-26 Peptide agonists of prostate-specific antigen and uses therefor

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US33466901P 2001-11-30 2001-11-30
US33457501P 2001-11-30 2001-11-30
US60/334,669 2001-11-30
US60/334,575 2001-11-30

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CA (1) CA2468258C (fr)
DE (1) DE60235041D1 (fr)
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Publication number Priority date Publication date Assignee Title
WO2005019464A1 (fr) * 2003-08-21 2005-03-03 Virax Development Pty Ltd Vecteur du poxvirus codant des antigenes specifiques de la prostate pour le traitement du cancer de la prostate
JP2007507521A (ja) * 2003-09-30 2007-03-29 ラドウィック インスティテュート フォア キャンサー リサーチ ＮＹ−ＥＳＯ−１とアジュバントのｉｎｖｉｖｏ有効性
JP2008526686A (ja) * 2004-11-16 2008-07-24 セントロ ド インムノロジア モレキュラー インターロイキン−２の中和能を有する免疫治療用製剤
US8703484B2 (en) 2005-05-05 2014-04-22 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Methods and compositions for detecting immune responses
US9575053B2 (en) 2012-03-30 2017-02-21 Kyoto University Urinary biomarker for use in test for prostate cancer

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US7902121B2 (en) * 2001-07-02 2011-03-08 The Board Of Trustees Of The Leland Stanford Junior University MHC-antigen arrays for detection and characterization of immune responses
AU2007221255B2 (en) * 2006-02-24 2012-03-08 The Government Of The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services Immunogenic peptides and methods of use
US20080095790A1 (en) * 2006-10-24 2008-04-24 Perambakam Supriya M Methods of Treating Prostate Cancer
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BR112012005713A2 (pt) 2009-09-14 2019-09-24 Baylor Res Institute vacinas direcionadas a célula langerhans.
US8557777B2 (en) 2010-07-09 2013-10-15 The Board Of Trustees Of The University Of Illinois Methods for treating cancer using prostate specific antigen and tumor endothelial marker peptides
WO2012006634A2 (fr) * 2010-07-09 2012-01-12 The Board Of Trustees Of The University Of Illiniois Thérapie peptidique par antigène prostatique spécifique (psa)
BR112013020875A2 (pt) 2011-02-15 2019-09-24 Immune Design Corp método para indução de uma resposta imune específica para um imunógeno em um indivíduo.
JP6054942B2 (ja) 2011-04-08 2016-12-27 イミューン デザイン コーポレイション 免疫原性組成物、ならびに体液性および細胞性免疫応答を誘発するための該組成物の使用方法
WO2013019445A2 (fr) * 2011-07-29 2013-02-07 Health Research, Inc. Peptides anti-angiogènes et leurs utilisations
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Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6946133B1 (en) 1996-03-20 2005-09-20 The United States Of America As Represented By The Department Of Health And Human Services Prostate specific antigen oligo-epitope peptide
AU8259798A (en) * 1997-06-20 1999-01-04 George G Klee Method for detection of breast cancer
WO2001087325A1 (fr) 2000-05-12 2001-11-22 Northwest Biotherapeutics, Inc. Methode permettant d'augmenter la presentation de classe i d'antigenes exogenes par les cellules dendritiques humaines

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WO2005019464A1 (fr) * 2003-08-21 2005-03-03 Virax Development Pty Ltd Vecteur du poxvirus codant des antigenes specifiques de la prostate pour le traitement du cancer de la prostate
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JP2008526686A (ja) * 2004-11-16 2008-07-24 セントロ ド インムノロジア モレキュラー インターロイキン−２の中和能を有する免疫治療用製剤
US8703484B2 (en) 2005-05-05 2014-04-22 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Methods and compositions for detecting immune responses
US9575053B2 (en) 2012-03-30 2017-02-21 Kyoto University Urinary biomarker for use in test for prostate cancer

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AU2002352913B2 (en) 2008-05-29
ATE454447T1 (de) 2010-01-15
US7247615B2 (en) 2007-07-24
WO2003047506A3 (fr) 2004-07-15
JP4364643B2 (ja) 2009-11-18
DK1461073T3 (da) 2010-03-29
AU2002352913A1 (en) 2003-06-17
EP1461073A2 (fr) 2004-09-29
EP1461073A4 (fr) 2007-01-17
ES2337454T3 (es) 2010-04-26
CA2468258C (fr) 2011-10-11
DE60235041D1 (de) 2010-02-25
US20050054575A1 (en) 2005-03-10
JP2005511037A (ja) 2005-04-28
EP1461073B1 (fr) 2010-01-06
CA2468258A1 (fr) 2003-06-12

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